�ݺ�ߣshows by User: AnandButani

�ݺ�ߣshows by User: AnandButani / http://www.slideshare.net/images/logo.gif �ݺ�ߣshows by User: AnandButani / Tue, 14 Nov 2017 18:30:14 GMT �ݺ�ߣShare feed for �ݺ�ߣshows by User: AnandButani Financing - Investigator Payment Models & Best Budget Practices /slideshow/financing-investigator-payment-models-best-budget-practices-82065832/82065832 financing-investigatorpaymentmodelsbestbudgetpractices-170202200121-171114183014
Aside from being a vital part of medical advancement, a clinical trial is a complex and expensive business which requires great planning and strategy. One big part of a successful trial are the finances. Financing clinical trials is a task that involves careful planning, anticipation, and negotiation of costs, budgets, and compensation to investigators. Taking into consideration the great number of items, procedures, protocols, subjects, and visits, it can be challenging to not miss or forget an item when you're preparing your budget. Managing to get the necessary budget that you need for covering all costs of conducting a trial requires careful anticipation and great negotiation skills. When negotiating your budget and explaining all the costs and expenses to sponsors, you have to take into consideration the costs of paying your investigators. ]]>
Aside from being a vital part of medical advancement, a clinical trial is a complex and expensive business which requires great planning and strategy. One big part of a successful trial are the finances. Financing clinical trials is a task that involves careful planning, anticipation, and negotiation of costs, budgets, and compensation to investigators. Taking into consideration the great number of items, procedures, protocols, subjects, and visits, it can be challenging to not miss or forget an item when you're preparing your budget. Managing to get the necessary budget that you need for covering all costs of conducting a trial requires careful anticipation and great negotiation skills. When negotiating your budget and explaining all the costs and expenses to sponsors, you have to take into consideration the costs of paying your investigators. ]]> Tue, 14 Nov 2017 18:30:14 GMT /slideshow/financing-investigator-payment-models-best-budget-practices-82065832/82065832 AnandButani@slideshare.net(AnandButani) Financing - Investigator Payment Models & Best Budget Practices AnandButani Aside from being a vital part of medical advancement, a clinical trial is a complex and expensive business which requires great planning and strategy. One big part of a successful trial are the finances. Financing clinical trials is a task that involves careful planning, anticipation, and negotiation of costs, budgets, and compensation to investigators. Taking into consideration the great number of items, procedures, protocols, subjects, and visits, it can be challenging to not miss or forget an item when you're preparing your budget. Managing to get the necessary budget that you need for covering all costs of conducting a trial requires careful anticipation and great negotiation skills. When negotiating your budget and explaining all the costs and expenses to sponsors, you have to take into consideration the costs of paying your investigators. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/financing-investigatorpaymentmodelsbestbudgetpractices-170202200121-171114183014-thumbnail.jpg?width=120&height=120&fit=bounds" /> Aside from being a vital part of medical advancement, a clinical trial is a complex and expensive business which requires great planning and strategy. One big part of a successful trial are the finances. Financing clinical trials is a task that involves careful planning, anticipation, and negotiation of costs, budgets, and compensation to investigators. Taking into consideration the great number of items, procedures, protocols, subjects, and visits, it can be challenging to not miss or forget an item when you're preparing your budget. Managing to get the necessary budget that you need for covering all costs of conducting a trial requires careful anticipation and great negotiation skills. When negotiating your budget and explaining all the costs and expenses to sponsors, you have to take into consideration the costs of paying your investigators.

Financing - Investigator Payment Models & Best Budget Practices from Anand Butani

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0 Got Studies? A Quick Guide to Help You Get Clinical Research Studies /AnandButani/got-studies-a-quick-guide-to-help-you-get-clinical-research-studies ebook-gotstudies-guidetonewstudies-trialjoin-170202200529-171114182843
This guide will provide you with strategies and resources to find support for your clinical research. ]]>
This guide will provide you with strategies and resources to find support for your clinical research. ]]> Tue, 14 Nov 2017 18:28:43 GMT /AnandButani/got-studies-a-quick-guide-to-help-you-get-clinical-research-studies AnandButani@slideshare.net(AnandButani) Got Studies? A Quick Guide to Help You Get Clinical Research Studies AnandButani This guide will provide you with strategies and resources to find support for your clinical research. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ebook-gotstudies-guidetonewstudies-trialjoin-170202200529-171114182843-thumbnail.jpg?width=120&height=120&fit=bounds" /> This guide will provide you with strategies and resources to find support for your clinical research.

Got Studies? A Quick Guide to Help You Get Clinical Research Studies from Anand Butani

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0 5 Reasons We Help Lift Off Your Study /slideshow/5-reasons-we-help-lift-off-your-study-82065477/82065477 5reaonswehelpliftoffyourstudy-gifppt-170222192926-171114182403
5 Reasons We Help Lift Off Your Study]]>
5 Reasons We Help Lift Off Your Study]]> Tue, 14 Nov 2017 18:24:03 GMT /slideshow/5-reasons-we-help-lift-off-your-study-82065477/82065477 AnandButani@slideshare.net(AnandButani) 5 Reasons We Help Lift Off Your Study AnandButani 5 Reasons We Help Lift Off Your Study <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/5reaonswehelpliftoffyourstudy-gifppt-170222192926-171114182403-thumbnail.jpg?width=120&height=120&fit=bounds" /> 5 Reasons We Help Lift Off Your Study

5 Reasons We Help Lift Off Your Study from Anand Butani

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0 Clinical Project Manager: Leading Causes of Problem-Solving Inefficiencies /slideshow/clinical-project-manager-leading-causes-of-problemsolving-inefficiencies/82062785 clinicalprojectmanager-leadingcausesofproblem-solvinginefficiencies-171114174027
A Clinical Project Manager (CPM) job is a high-rank position in the research world that many CRAs and investigators are aiming to reach. Being a Clinical Project Manager entails careful thinking, planning, and managing all features of a trial or study. The CPM’s role is to act as a middleman between the sponsor and the site. This means that he or she will be responsible for managing and leading CRAs and other site medical specialists such as PIs, sub-investigators, nurses, coordinators, etc. ]]>
A Clinical Project Manager (CPM) job is a high-rank position in the research world that many CRAs and investigators are aiming to reach. Being a Clinical Project Manager entails careful thinking, planning, and managing all features of a trial or study. The CPM’s role is to act as a middleman between the sponsor and the site. This means that he or she will be responsible for managing and leading CRAs and other site medical specialists such as PIs, sub-investigators, nurses, coordinators, etc. ]]> Tue, 14 Nov 2017 17:40:27 GMT /slideshow/clinical-project-manager-leading-causes-of-problemsolving-inefficiencies/82062785 AnandButani@slideshare.net(AnandButani) Clinical Project Manager: Leading Causes of Problem-Solving Inefficiencies AnandButani A Clinical Project Manager (CPM) job is a high-rank position in the research world that many CRAs and investigators are aiming to reach. Being a Clinical Project Manager entails careful thinking, planning, and managing all features of a trial or study. The CPM’s role is to act as a middleman between the sponsor and the site. This means that he or she will be responsible for managing and leading CRAs and other site medical specialists such as PIs, sub-investigators, nurses, coordinators, etc. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/clinicalprojectmanager-leadingcausesofproblem-solvinginefficiencies-171114174027-thumbnail.jpg?width=120&height=120&fit=bounds" /> A Clinical Project Manager (CPM) job is a high-rank position in the research world that many CRAs and investigators are aiming to reach. Being a Clinical Project Manager entails careful thinking, planning, and managing all features of a trial or study. The CPM’s role is to act as a middleman between the sponsor and the site. This means that he or she will be responsible for managing and leading CRAs and other site medical specialists such as PIs, sub-investigators, nurses, coordinators, etc.

Clinical Project Manager: Leading Causes of Problem-Solving Inefficiencies from Anand Butani

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0 Diabetes Comprehensive Guide /AnandButani/diabetes-comprehensive-guide copyofebook-diabetescomprehensiveguide-171114173733
Chapter 1: An Overview of the Disease Chapter 2: What are the Types of Diabetes? Chapter 3: What are the Symptoms of Diabetes? Chapter 4: What are the Causes of the Two Major Types of Diabetes? Chapter 5: Diabetes Comorbidities and Complications Chapter 6: What is Diabetic Neuropathy? Chapter 7: The Diabetic Pregnant Woman and Her Offspring Chapter 8: Treatments for Diabetes Chapter 9: The Diabetic Diet: Carbohydrates and Glycemic Index Chapter 10: Other Things that Could Help a Diabetic Person Chapter 11: Diabetes Myths and Truths ]]>
Chapter 1: An Overview of the Disease Chapter 2: What are the Types of Diabetes? Chapter 3: What are the Symptoms of Diabetes? Chapter 4: What are the Causes of the Two Major Types of Diabetes? Chapter 5: Diabetes Comorbidities and Complications Chapter 6: What is Diabetic Neuropathy? Chapter 7: The Diabetic Pregnant Woman and Her Offspring Chapter 8: Treatments for Diabetes Chapter 9: The Diabetic Diet: Carbohydrates and Glycemic Index Chapter 10: Other Things that Could Help a Diabetic Person Chapter 11: Diabetes Myths and Truths ]]> Tue, 14 Nov 2017 17:37:33 GMT /AnandButani/diabetes-comprehensive-guide AnandButani@slideshare.net(AnandButani) Diabetes Comprehensive Guide AnandButani Chapter 1: An Overview of the Disease Chapter 2: What are the Types of Diabetes? Chapter 3: What are the Symptoms of Diabetes? Chapter 4: What are the Causes of the Two Major Types of Diabetes? Chapter 5: Diabetes Comorbidities and Complications Chapter 6: What is Diabetic Neuropathy? Chapter 7: The Diabetic Pregnant Woman and Her Offspring Chapter 8: Treatments for Diabetes Chapter 9: The Diabetic Diet: Carbohydrates and Glycemic Index Chapter 10: Other Things that Could Help a Diabetic Person Chapter 11: Diabetes Myths and Truths <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/copyofebook-diabetescomprehensiveguide-171114173733-thumbnail.jpg?width=120&height=120&fit=bounds" /> Chapter 1: An Overview of the Disease Chapter 2: What are the Types of Diabetes? Chapter 3: What are the Symptoms of Diabetes? Chapter 4: What are the Causes of the Two Major Types of Diabetes? Chapter 5: Diabetes Comorbidities and Complications Chapter 6: What is Diabetic Neuropathy? Chapter 7: The Diabetic Pregnant Woman and Her Offspring Chapter 8: Treatments for Diabetes Chapter 9: The Diabetic Diet: Carbohydrates and Glycemic Index Chapter 10: Other Things that Could Help a Diabetic Person Chapter 11: Diabetes Myths and Truths

Diabetes Comprehensive Guide from Anand Butani

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0 CTMS for Your Site's Financial Activities /slideshow/ctms-for-your-sites-financial-activities-82062336/82062336 ctmsforyoursitesfinancialactivities-171114173312
- Accurately tracking and managing financials is important for your site's successful conducting of a trial, as well as the site's general success in the long-run. - There are 2 possible outcomes by not taking proper care of your site's financial activities, either you're losing unaccounted money or you're spending a lot of unnecessary time and effort to make sure you're not missing anything. - Sites nowadays use electronic systems for financial management such as a CTMS (clinical trial management system). ]]>
- Accurately tracking and managing financials is important for your site's successful conducting of a trial, as well as the site's general success in the long-run. - There are 2 possible outcomes by not taking proper care of your site's financial activities, either you're losing unaccounted money or you're spending a lot of unnecessary time and effort to make sure you're not missing anything. - Sites nowadays use electronic systems for financial management such as a CTMS (clinical trial management system). ]]> Tue, 14 Nov 2017 17:33:12 GMT /slideshow/ctms-for-your-sites-financial-activities-82062336/82062336 AnandButani@slideshare.net(AnandButani) CTMS for Your Site's Financial Activities AnandButani - Accurately tracking and managing financials is important for your site's successful conducting of a trial, as well as the site's general success in the long-run. - There are 2 possible outcomes by not taking proper care of your site's financial activities, either you're losing unaccounted money or you're spending a lot of unnecessary time and effort to make sure you're not missing anything. - Sites nowadays use electronic systems for financial management such as a CTMS (clinical trial management system). <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ctmsforyoursitesfinancialactivities-171114173312-thumbnail.jpg?width=120&height=120&fit=bounds" /> - Accurately tracking and managing financials is important for your site's successful conducting of a trial, as well as the site's general success in the long-run. - There are 2 possible outcomes by not taking proper care of your site's financial activities, either you're losing unaccounted money or you're spending a lot of unnecessary time and effort to make sure you're not missing anything. - Sites nowadays use electronic systems for financial management such as a CTMS (clinical trial management system).

CTMS for Your Site's Financial Activities from Anand Butani

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0 Drug Accountability: An Important Aspect of Clinical Research /slideshow/drug-accountability-an-important-aspect-of-clinical-research-82062221/82062221 drugaccountability-animportantaspectofclinicalresearch-171114173122
Drug accountability is an interesting topic related to clinical research, both for the CRAs and for the clinical research sites. Even though drug accountability isn’t a task that should be performed by the CRA, he or she is still responsible for monitoring and making sure that the site is correctly performing every task related to this field. The topic of drug accountability is especially important in regards to quality data as well as for patient safety. For this reason, we’ll give you an in-depth explanation of everything that drug accountability entails. ]]>
Drug accountability is an interesting topic related to clinical research, both for the CRAs and for the clinical research sites. Even though drug accountability isn’t a task that should be performed by the CRA, he or she is still responsible for monitoring and making sure that the site is correctly performing every task related to this field. The topic of drug accountability is especially important in regards to quality data as well as for patient safety. For this reason, we’ll give you an in-depth explanation of everything that drug accountability entails. ]]> Tue, 14 Nov 2017 17:31:22 GMT /slideshow/drug-accountability-an-important-aspect-of-clinical-research-82062221/82062221 AnandButani@slideshare.net(AnandButani) Drug Accountability: An Important Aspect of Clinical Research AnandButani Drug accountability is an interesting topic related to clinical research, both for the CRAs and for the clinical research sites. Even though drug accountability isn’t a task that should be performed by the CRA, he or she is still responsible for monitoring and making sure that the site is correctly performing every task related to this field. The topic of drug accountability is especially important in regards to quality data as well as for patient safety. For this reason, we’ll give you an in-depth explanation of everything that drug accountability entails. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/drugaccountability-animportantaspectofclinicalresearch-171114173122-thumbnail.jpg?width=120&height=120&fit=bounds" /> Drug accountability is an interesting topic related to clinical research, both for the CRAs and for the clinical research sites. Even though drug accountability isn’t a task that should be performed by the CRA, he or she is still responsible for monitoring and making sure that the site is correctly performing every task related to this field. The topic of drug accountability is especially important in regards to quality data as well as for patient safety. For this reason, we’ll give you an in-depth explanation of everything that drug accountability entails.

Drug Accountability: An Important Aspect of Clinical Research from Anand Butani

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0 Essential Regulatory Documents in Clinical Trials /slideshow/essential-regulatory-documents-in-clinical-trials-82062180/82062180 essentialregulatorydocumentsinclinicaltrials-171114173039
Maintaining and storing the essential regulatory documents is an important practice in clinical research. The proper filing and organization of these documents can greatly improve a clinical trial management. Usually, Regulatory Documents will be stored in a binder (or binders) that’s provided to the site for that specific study. Filling out these documents and filing them properly is the site’s and especially the PI’s responsibility. Storing them properly is also the site’s responsibility, not the CRA’s. In any case, after the study is over, the sponsor or the CRO will inform the site if they should keep the originals or make copies of the Regulatory Documents for storage. Similarly, the sponsor or the CRO will also tell the site how long they need the documents to be kept and stored on-site. ]]>
Maintaining and storing the essential regulatory documents is an important practice in clinical research. The proper filing and organization of these documents can greatly improve a clinical trial management. Usually, Regulatory Documents will be stored in a binder (or binders) that’s provided to the site for that specific study. Filling out these documents and filing them properly is the site’s and especially the PI’s responsibility. Storing them properly is also the site’s responsibility, not the CRA’s. In any case, after the study is over, the sponsor or the CRO will inform the site if they should keep the originals or make copies of the Regulatory Documents for storage. Similarly, the sponsor or the CRO will also tell the site how long they need the documents to be kept and stored on-site. ]]> Tue, 14 Nov 2017 17:30:39 GMT /slideshow/essential-regulatory-documents-in-clinical-trials-82062180/82062180 AnandButani@slideshare.net(AnandButani) Essential Regulatory Documents in Clinical Trials AnandButani Maintaining and storing the essential regulatory documents is an important practice in clinical research. The proper filing and organization of these documents can greatly improve a clinical trial management. Usually, Regulatory Documents will be stored in a binder (or binders) that’s provided to the site for that specific study. Filling out these documents and filing them properly is the site’s and especially the PI’s responsibility. Storing them properly is also the site’s responsibility, not the CRA’s. In any case, after the study is over, the sponsor or the CRO will inform the site if they should keep the originals or make copies of the Regulatory Documents for storage. Similarly, the sponsor or the CRO will also tell the site how long they need the documents to be kept and stored on-site. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/essentialregulatorydocumentsinclinicaltrials-171114173039-thumbnail.jpg?width=120&height=120&fit=bounds" /> Maintaining and storing the essential regulatory documents is an important practice in clinical research. The proper filing and organization of these documents can greatly improve a clinical trial management. Usually, Regulatory Documents will be stored in a binder (or binders) that’s provided to the site for that specific study. Filling out these documents and filing them properly is the site’s and especially the PI’s responsibility. Storing them properly is also the site’s responsibility, not the CRA’s. In any case, after the study is over, the sponsor or the CRO will inform the site if they should keep the originals or make copies of the Regulatory Documents for storage. Similarly, the sponsor or the CRO will also tell the site how long they need the documents to be kept and stored on-site.

Essential Regulatory Documents in Clinical Trials from Anand Butani

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0 Essentials for Setting up a New Clinical Research Center /slideshow/essentials-for-setting-up-a-new-clinical-research-center-82062114/82062114 essentialsforsettingupanewclinicalresearchcenter-171114172928
This one is for all the doctors and medical specialists who are interested in opening up their own research clinic. As a doctor who’s interested in this option, we imagine that you’ve already seen a clinical research environment either by participating as a sub-investigator or a PI (principal investigator). If this is the case and you’re already familiar with everything that clinical research entails, then you’re in a good position to start your own clinical research center or research clinic. ]]>
This one is for all the doctors and medical specialists who are interested in opening up their own research clinic. As a doctor who’s interested in this option, we imagine that you’ve already seen a clinical research environment either by participating as a sub-investigator or a PI (principal investigator). If this is the case and you’re already familiar with everything that clinical research entails, then you’re in a good position to start your own clinical research center or research clinic. ]]> Tue, 14 Nov 2017 17:29:27 GMT /slideshow/essentials-for-setting-up-a-new-clinical-research-center-82062114/82062114 AnandButani@slideshare.net(AnandButani) Essentials for Setting up a New Clinical Research Center AnandButani This one is for all the doctors and medical specialists who are interested in opening up their own research clinic. As a doctor who’s interested in this option, we imagine that you’ve already seen a clinical research environment either by participating as a sub-investigator or a PI (principal investigator). If this is the case and you’re already familiar with everything that clinical research entails, then you’re in a good position to start your own clinical research center or research clinic. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/essentialsforsettingupanewclinicalresearchcenter-171114172928-thumbnail.jpg?width=120&height=120&fit=bounds" /> This one is for all the doctors and medical specialists who are interested in opening up their own research clinic. As a doctor who’s interested in this option, we imagine that you’ve already seen a clinical research environment either by participating as a sub-investigator or a PI (principal investigator). If this is the case and you’re already familiar with everything that clinical research entails, then you’re in a good position to start your own clinical research center or research clinic.

Essentials for Setting up a New Clinical Research Center from Anand Butani

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0 Explaining the Different Types of Routine Monitoring Visits /slideshow/explaining-the-different-types-of-routine-monitoring-visits-82062045/82062045 explainingthedifferenttypesofroutinemonitoringvisits-171114172827
In the clinical research industry, there are several types of basic monitoring visits that everyone involved in it should differentiate, especially CRAs (monitors). A CRA (clinical research associate) or a monitor is the person responsible for visiting a site in order to ensure that the clinical trial is being conducted properly. The CRA’s tasks include on-site visits and ensuring compliance, subjects’ safety, data quality and integrity, etc. Although clinical trials belong in the medical field, a CRA doesn’t have to be a doctor or a medical professional. It’s enough if a CRA has a background in Life Sciences, past experience in clinical trials (most often as a coordinator), and the proper training. The main monitoring visits are the Site Selection Visit, Site Initiation Visit, Regular (Interim) Monitoring Visits, Site Close-Out Visit, and the Pre-Audit Visit. Out of all these monitoring visits, here we’ll pay more attention to the Routine Monitoring Visits, as one of the most frequent and important visits at a site. ]]>
In the clinical research industry, there are several types of basic monitoring visits that everyone involved in it should differentiate, especially CRAs (monitors). A CRA (clinical research associate) or a monitor is the person responsible for visiting a site in order to ensure that the clinical trial is being conducted properly. The CRA’s tasks include on-site visits and ensuring compliance, subjects’ safety, data quality and integrity, etc. Although clinical trials belong in the medical field, a CRA doesn’t have to be a doctor or a medical professional. It’s enough if a CRA has a background in Life Sciences, past experience in clinical trials (most often as a coordinator), and the proper training. The main monitoring visits are the Site Selection Visit, Site Initiation Visit, Regular (Interim) Monitoring Visits, Site Close-Out Visit, and the Pre-Audit Visit. Out of all these monitoring visits, here we’ll pay more attention to the Routine Monitoring Visits, as one of the most frequent and important visits at a site. ]]> Tue, 14 Nov 2017 17:28:27 GMT /slideshow/explaining-the-different-types-of-routine-monitoring-visits-82062045/82062045 AnandButani@slideshare.net(AnandButani) Explaining the Different Types of Routine Monitoring Visits AnandButani In the clinical research industry, there are several types of basic monitoring visits that everyone involved in it should differentiate, especially CRAs (monitors). A CRA (clinical research associate) or a monitor is the person responsible for visiting a site in order to ensure that the clinical trial is being conducted properly. The CRA’s tasks include on-site visits and ensuring compliance, subjects’ safety, data quality and integrity, etc. Although clinical trials belong in the medical field, a CRA doesn’t have to be a doctor or a medical professional. It’s enough if a CRA has a background in Life Sciences, past experience in clinical trials (most often as a coordinator), and the proper training. The main monitoring visits are the Site Selection Visit, Site Initiation Visit, Regular (Interim) Monitoring Visits, Site Close-Out Visit, and the Pre-Audit Visit. Out of all these monitoring visits, here we’ll pay more attention to the Routine Monitoring Visits, as one of the most frequent and important visits at a site. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/explainingthedifferenttypesofroutinemonitoringvisits-171114172827-thumbnail.jpg?width=120&height=120&fit=bounds" /> In the clinical research industry, there are several types of basic monitoring visits that everyone involved in it should differentiate, especially CRAs (monitors). A CRA (clinical research associate) or a monitor is the person responsible for visiting a site in order to ensure that the clinical trial is being conducted properly. The CRA’s tasks include on-site visits and ensuring compliance, subjects’ safety, data quality and integrity, etc. Although clinical trials belong in the medical field, a CRA doesn’t have to be a doctor or a medical professional. It’s enough if a CRA has a background in Life Sciences, past experience in clinical trials (most often as a coordinator), and the proper training. The main monitoring visits are the Site Selection Visit, Site Initiation Visit, Regular (Interim) Monitoring Visits, Site Close-Out Visit, and the Pre-Audit Visit. Out of all these monitoring visits, here we’ll pay more attention to the Routine Monitoring Visits, as one of the most frequent and important visits at a site.

Explaining the Different Types of Routine Monitoring Visits from Anand Butani

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0 Helpful Information on Getting a Clinical Research Job as a CRA /slideshow/helpful-information-on-getting-a-clinical-research-job-as-a-cra-82061760/82061760 helpfulinformationongettingaclinicalresearchjobasacra-171114172335
Clinical research is nowadays considered to be a fast-growing business, so many people are trying to look for ways to enter. There are many work positions in a clinical research facility, all depending on your experience and qualifications. If you’re reading this, then probably you’re also interested in getting a clinical-research-related job position. And that’s great because this article is exactly for you! Next, we’ll help you prepare for a job interview in clinical research, no matter which position you’re applying for! People who are interested in this field, are usually trying to get a job as a study coordinator, a CRA, or a research assistant. However, the strategies and tips we’ll give you can be applied to any research-related job! ]]>
Clinical research is nowadays considered to be a fast-growing business, so many people are trying to look for ways to enter. There are many work positions in a clinical research facility, all depending on your experience and qualifications. If you’re reading this, then probably you’re also interested in getting a clinical-research-related job position. And that’s great because this article is exactly for you! Next, we’ll help you prepare for a job interview in clinical research, no matter which position you’re applying for! People who are interested in this field, are usually trying to get a job as a study coordinator, a CRA, or a research assistant. However, the strategies and tips we’ll give you can be applied to any research-related job! ]]> Tue, 14 Nov 2017 17:23:35 GMT /slideshow/helpful-information-on-getting-a-clinical-research-job-as-a-cra-82061760/82061760 AnandButani@slideshare.net(AnandButani) Helpful Information on Getting a Clinical Research Job as a CRA AnandButani Clinical research is nowadays considered to be a fast-growing business, so many people are trying to look for ways to enter. There are many work positions in a clinical research facility, all depending on your experience and qualifications. If you’re reading this, then probably you’re also interested in getting a clinical-research-related job position. And that’s great because this article is exactly for you! Next, we’ll help you prepare for a job interview in clinical research, no matter which position you’re applying for! People who are interested in this field, are usually trying to get a job as a study coordinator, a CRA, or a research assistant. However, the strategies and tips we’ll give you can be applied to any research-related job! <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/helpfulinformationongettingaclinicalresearchjobasacra-171114172335-thumbnail.jpg?width=120&height=120&fit=bounds" /> Clinical research is nowadays considered to be a fast-growing business, so many people are trying to look for ways to enter. There are many work positions in a clinical research facility, all depending on your experience and qualifications. If you’re reading this, then probably you’re also interested in getting a clinical-research-related job position. And that’s great because this article is exactly for you! Next, we’ll help you prepare for a job interview in clinical research, no matter which position you’re applying for! People who are interested in this field, are usually trying to get a job as a study coordinator, a CRA, or a research assistant. However, the strategies and tips we’ll give you can be applied to any research-related job!

Helpful Information on Getting a Clinical Research Job as a CRA from Anand Butani

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0 Monitoring Plan and Basic Monitoring Visits: Everything that a CRA Needs to Know /slideshow/monitoring-plan-and-basic-monitoring-visits-everything-that-a-cra-needs-to-know-82061523/82061523 monitoringplanandbasicmonitoringvisits-everythingthatacraneedstoknow-171114171948
A monitor in a clinical trial is also called a CRA - clinical research associate. This person is a professional who’s responsible for monitoring the clinical trial and making sure that everything is according to rules, regulations, and good clinical practice. Whether you already are a CRA or you’re trying to become one, the most important thing you should be aware of is the monitoring plan. You, as a CRA or a future CRA, should know what a monitoring plan is, what it serves for, and what it consists of. The second most important information for you are the monitoring visits. Below, we’ll explain all the components of a monitoring plan, as well as which are the most basic and important monitoring visits. ]]>
A monitor in a clinical trial is also called a CRA - clinical research associate. This person is a professional who’s responsible for monitoring the clinical trial and making sure that everything is according to rules, regulations, and good clinical practice. Whether you already are a CRA or you’re trying to become one, the most important thing you should be aware of is the monitoring plan. You, as a CRA or a future CRA, should know what a monitoring plan is, what it serves for, and what it consists of. The second most important information for you are the monitoring visits. Below, we’ll explain all the components of a monitoring plan, as well as which are the most basic and important monitoring visits. ]]> Tue, 14 Nov 2017 17:19:48 GMT /slideshow/monitoring-plan-and-basic-monitoring-visits-everything-that-a-cra-needs-to-know-82061523/82061523 AnandButani@slideshare.net(AnandButani) Monitoring Plan and Basic Monitoring Visits: Everything that a CRA Needs to Know AnandButani A monitor in a clinical trial is also called a CRA - clinical research associate. This person is a professional who’s responsible for monitoring the clinical trial and making sure that everything is according to rules, regulations, and good clinical practice. Whether you already are a CRA or you’re trying to become one, the most important thing you should be aware of is the monitoring plan. You, as a CRA or a future CRA, should know what a monitoring plan is, what it serves for, and what it consists of. The second most important information for you are the monitoring visits. Below, we’ll explain all the components of a monitoring plan, as well as which are the most basic and important monitoring visits. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/monitoringplanandbasicmonitoringvisits-everythingthatacraneedstoknow-171114171948-thumbnail.jpg?width=120&height=120&fit=bounds" /> A monitor in a clinical trial is also called a CRA - clinical research associate. This person is a professional who’s responsible for monitoring the clinical trial and making sure that everything is according to rules, regulations, and good clinical practice. Whether you already are a CRA or you’re trying to become one, the most important thing you should be aware of is the monitoring plan. You, as a CRA or a future CRA, should know what a monitoring plan is, what it serves for, and what it consists of. The second most important information for you are the monitoring visits. Below, we’ll explain all the components of a monitoring plan, as well as which are the most basic and important monitoring visits.

Monitoring Plan and Basic Monitoring Visits: Everything that a CRA Needs to Know from Anand Butani

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0 Most Common Clinical Research Site Worries and Complaints /slideshow/most-common-clinical-research-site-worries-and-complaints-82061471/82061471 mostcommonclinicalresearchsiteworriesandcomplaints-171114171858
All clinical research sites, especially new ones who’ve just entered the business, have a couple of common worries and complaints. The clinical research field is complicated and there are tons of formalities, papers, vendors, rules, regulations, etc. Taking into consideration the sensitivity of this business, the fact that human participants are involved, as well as the large amount of money that sponsors spend on a research, we have to work as professionally as possible. There are many steps involved in a clinical trial, starting from the site selection visit, negotiations, then routine monitoring visits, subject enrollment and randomization, etc. All of these steps are equally important in order to conduct a successful trial. However, the complexity of the clinical research process usually worries and confuses new research sites. We’ve done a research on some of the most common site worries and complaints throughout the duration of a trial. Below, we’ll give you answers to all your questions. ]]>
All clinical research sites, especially new ones who’ve just entered the business, have a couple of common worries and complaints. The clinical research field is complicated and there are tons of formalities, papers, vendors, rules, regulations, etc. Taking into consideration the sensitivity of this business, the fact that human participants are involved, as well as the large amount of money that sponsors spend on a research, we have to work as professionally as possible. There are many steps involved in a clinical trial, starting from the site selection visit, negotiations, then routine monitoring visits, subject enrollment and randomization, etc. All of these steps are equally important in order to conduct a successful trial. However, the complexity of the clinical research process usually worries and confuses new research sites. We’ve done a research on some of the most common site worries and complaints throughout the duration of a trial. Below, we’ll give you answers to all your questions. ]]> Tue, 14 Nov 2017 17:18:58 GMT /slideshow/most-common-clinical-research-site-worries-and-complaints-82061471/82061471 AnandButani@slideshare.net(AnandButani) Most Common Clinical Research Site Worries and Complaints AnandButani All clinical research sites, especially new ones who’ve just entered the business, have a couple of common worries and complaints. The clinical research field is complicated and there are tons of formalities, papers, vendors, rules, regulations, etc. Taking into consideration the sensitivity of this business, the fact that human participants are involved, as well as the large amount of money that sponsors spend on a research, we have to work as professionally as possible. There are many steps involved in a clinical trial, starting from the site selection visit, negotiations, then routine monitoring visits, subject enrollment and randomization, etc. All of these steps are equally important in order to conduct a successful trial. However, the complexity of the clinical research process usually worries and confuses new research sites. We’ve done a research on some of the most common site worries and complaints throughout the duration of a trial. Below, we’ll give you answers to all your questions. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/mostcommonclinicalresearchsiteworriesandcomplaints-171114171858-thumbnail.jpg?width=120&height=120&fit=bounds" /> All clinical research sites, especially new ones who’ve just entered the business, have a couple of common worries and complaints. The clinical research field is complicated and there are tons of formalities, papers, vendors, rules, regulations, etc. Taking into consideration the sensitivity of this business, the fact that human participants are involved, as well as the large amount of money that sponsors spend on a research, we have to work as professionally as possible. There are many steps involved in a clinical trial, starting from the site selection visit, negotiations, then routine monitoring visits, subject enrollment and randomization, etc. All of these steps are equally important in order to conduct a successful trial. However, the complexity of the clinical research process usually worries and confuses new research sites. We’ve done a research on some of the most common site worries and complaints throughout the duration of a trial. Below, we’ll give you answers to all your questions.

Most Common Clinical Research Site Worries and Complaints from Anand Butani

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0 New Drug Application: How to Speed Up FDA Approval /slideshow/new-drug-application-how-to-speed-up-fda-approval-82061264/82061264 newdrugapplication-howtospeedupfdaapproval-171114171548
We all know that sponsors invest a lot of money in animal and human clinical studies where they test the safety and efficiency of a new drug. Sites are chosen which conduct the trials and in the end, they gather data for further analysis. But, what’s the purpose of it all? What happens after the trials end? ]]>
We all know that sponsors invest a lot of money in animal and human clinical studies where they test the safety and efficiency of a new drug. Sites are chosen which conduct the trials and in the end, they gather data for further analysis. But, what’s the purpose of it all? What happens after the trials end? ]]> Tue, 14 Nov 2017 17:15:48 GMT /slideshow/new-drug-application-how-to-speed-up-fda-approval-82061264/82061264 AnandButani@slideshare.net(AnandButani) New Drug Application: How to Speed Up FDA Approval AnandButani We all know that sponsors invest a lot of money in animal and human clinical studies where they test the safety and efficiency of a new drug. Sites are chosen which conduct the trials and in the end, they gather data for further analysis. But, what’s the purpose of it all? What happens after the trials end? <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/newdrugapplication-howtospeedupfdaapproval-171114171548-thumbnail.jpg?width=120&height=120&fit=bounds" /> We all know that sponsors invest a lot of money in animal and human clinical studies where they test the safety and efficiency of a new drug. Sites are chosen which conduct the trials and in the end, they gather data for further analysis. But, what’s the purpose of it all? What happens after the trials end?

New Drug Application: How to Speed Up FDA Approval from Anand Butani

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0 Regulations in Clinical Research: Obligations and Responsibilities of Investigators /AnandButani/regulations-in-clinical-research-obligations-and-responsibilities-of-investigators-82061119 regulationsinclinicalresearch-obligationsandresponsibilitiesofinvestigators-171114171331
Two of the most important individuals in a clinical trial are investigators and sponsors. However, being such a crucial part of a trial also brings many obligations and responsibilities. Although the sponsor is the one who initiates and finances a trial, the investigator is the person who conducts it. For this reason, most of the obligations and responsibilities fall on the investigator as the person accountable for everything that goes wrong in a trial. Learning these obligations and knowing how to follow them is a crucial practice that will ensure compliance in a clinical trial. For this reason, we’ve decided to compose this material that will give you a basic outline of all the rules and regulations that investigators and sponsors should follow. ]]>
Two of the most important individuals in a clinical trial are investigators and sponsors. However, being such a crucial part of a trial also brings many obligations and responsibilities. Although the sponsor is the one who initiates and finances a trial, the investigator is the person who conducts it. For this reason, most of the obligations and responsibilities fall on the investigator as the person accountable for everything that goes wrong in a trial. Learning these obligations and knowing how to follow them is a crucial practice that will ensure compliance in a clinical trial. For this reason, we’ve decided to compose this material that will give you a basic outline of all the rules and regulations that investigators and sponsors should follow. ]]> Tue, 14 Nov 2017 17:13:31 GMT /AnandButani/regulations-in-clinical-research-obligations-and-responsibilities-of-investigators-82061119 AnandButani@slideshare.net(AnandButani) Regulations in Clinical Research: Obligations and Responsibilities of Investigators AnandButani Two of the most important individuals in a clinical trial are investigators and sponsors. However, being such a crucial part of a trial also brings many obligations and responsibilities. Although the sponsor is the one who initiates and finances a trial, the investigator is the person who conducts it. For this reason, most of the obligations and responsibilities fall on the investigator as the person accountable for everything that goes wrong in a trial. Learning these obligations and knowing how to follow them is a crucial practice that will ensure compliance in a clinical trial. For this reason, we’ve decided to compose this material that will give you a basic outline of all the rules and regulations that investigators and sponsors should follow. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/regulationsinclinicalresearch-obligationsandresponsibilitiesofinvestigators-171114171331-thumbnail.jpg?width=120&height=120&fit=bounds" /> Two of the most important individuals in a clinical trial are investigators and sponsors. However, being such a crucial part of a trial also brings many obligations and responsibilities. Although the sponsor is the one who initiates and finances a trial, the investigator is the person who conducts it. For this reason, most of the obligations and responsibilities fall on the investigator as the person accountable for everything that goes wrong in a trial. Learning these obligations and knowing how to follow them is a crucial practice that will ensure compliance in a clinical trial. For this reason, we’ve decided to compose this material that will give you a basic outline of all the rules and regulations that investigators and sponsors should follow.

Regulations in Clinical Research: Obligations and Responsibilities of Investigators from Anand Butani

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0 Standard Of Care Costs vs Study-Related Costs /slideshow/standard-of-care-costs-vs-studyrelated-costs-82060971/82060971 standardofcarecostsvsstudy-relatedcosts-171114171127
In order for a study to be conducted properly, the sponsor and the site have to negotiate a fair and mutually agreeable budget. When we’re talking about budgeting for a study, there are many separate items and things to be considered. One of the most intriguing points in a budget is the difference between Standard of Care costs and Research-Specific (study-related) costs. Clinical research is an area where it’s required that the sponsors disclose every dollar and every single amount which they pay to doctors they work with, and for this reason, calculating the standard of care costs is important when preparing the budget for a study. Here, we’ll help you differentiate standard of care costs and study-related costs, so that you are able to prepare your budget in the best way possible. ]]>
In order for a study to be conducted properly, the sponsor and the site have to negotiate a fair and mutually agreeable budget. When we’re talking about budgeting for a study, there are many separate items and things to be considered. One of the most intriguing points in a budget is the difference between Standard of Care costs and Research-Specific (study-related) costs. Clinical research is an area where it’s required that the sponsors disclose every dollar and every single amount which they pay to doctors they work with, and for this reason, calculating the standard of care costs is important when preparing the budget for a study. Here, we’ll help you differentiate standard of care costs and study-related costs, so that you are able to prepare your budget in the best way possible. ]]> Tue, 14 Nov 2017 17:11:27 GMT /slideshow/standard-of-care-costs-vs-studyrelated-costs-82060971/82060971 AnandButani@slideshare.net(AnandButani) Standard Of Care Costs vs Study-Related Costs AnandButani In order for a study to be conducted properly, the sponsor and the site have to negotiate a fair and mutually agreeable budget. When we’re talking about budgeting for a study, there are many separate items and things to be considered. One of the most intriguing points in a budget is the difference between Standard of Care costs and Research-Specific (study-related) costs. Clinical research is an area where it’s required that the sponsors disclose every dollar and every single amount which they pay to doctors they work with, and for this reason, calculating the standard of care costs is important when preparing the budget for a study. Here, we’ll help you differentiate standard of care costs and study-related costs, so that you are able to prepare your budget in the best way possible. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/standardofcarecostsvsstudy-relatedcosts-171114171127-thumbnail.jpg?width=120&height=120&fit=bounds" /> In order for a study to be conducted properly, the sponsor and the site have to negotiate a fair and mutually agreeable budget. When we’re talking about budgeting for a study, there are many separate items and things to be considered. One of the most intriguing points in a budget is the difference between Standard of Care costs and Research-Specific (study-related) costs. Clinical research is an area where it’s required that the sponsors disclose every dollar and every single amount which they pay to doctors they work with, and for this reason, calculating the standard of care costs is important when preparing the budget for a study. Here, we’ll help you differentiate standard of care costs and study-related costs, so that you are able to prepare your budget in the best way possible.

Standard Of Care Costs vs Study-Related Costs from Anand Butani

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0 Types and Designs of Clinical Studies /slideshow/types-and-designs-of-clinical-studies-82060826/82060826 typesanddesignsofclinicalstudies-171114170930
Clinical study types and designs are terms which represent the way in which clinical trials are structured and formulated. Since we all know that clinical research is an extremely complex topic and not everything can be explained in a simple way, here we’ll focus only on some of the most basic types of clinical study types and designs which involve human subjects or participants. First of all, you should know that the most basic grouping of study designs is experimental (treatment) studies and observational studies. As we can suppose from the names, in an observational study, researchers have less control over subjects and they’re just observing what happens to subjects, while in experimental studies, researchers are using different methods (such as randomization) to place subjects in separate groups. This gives experimental studies much more validity than observational studies. In this guide, we’ll talk about the 2 possible types of studies, as well as different study designs within. ]]>
Clinical study types and designs are terms which represent the way in which clinical trials are structured and formulated. Since we all know that clinical research is an extremely complex topic and not everything can be explained in a simple way, here we’ll focus only on some of the most basic types of clinical study types and designs which involve human subjects or participants. First of all, you should know that the most basic grouping of study designs is experimental (treatment) studies and observational studies. As we can suppose from the names, in an observational study, researchers have less control over subjects and they’re just observing what happens to subjects, while in experimental studies, researchers are using different methods (such as randomization) to place subjects in separate groups. This gives experimental studies much more validity than observational studies. In this guide, we’ll talk about the 2 possible types of studies, as well as different study designs within. ]]> Tue, 14 Nov 2017 17:09:30 GMT /slideshow/types-and-designs-of-clinical-studies-82060826/82060826 AnandButani@slideshare.net(AnandButani) Types and Designs of Clinical Studies AnandButani Clinical study types and designs are terms which represent the way in which clinical trials are structured and formulated. Since we all know that clinical research is an extremely complex topic and not everything can be explained in a simple way, here we’ll focus only on some of the most basic types of clinical study types and designs which involve human subjects or participants. First of all, you should know that the most basic grouping of study designs is experimental (treatment) studies and observational studies. As we can suppose from the names, in an observational study, researchers have less control over subjects and they’re just observing what happens to subjects, while in experimental studies, researchers are using different methods (such as randomization) to place subjects in separate groups. This gives experimental studies much more validity than observational studies. In this guide, we’ll talk about the 2 possible types of studies, as well as different study designs within. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/typesanddesignsofclinicalstudies-171114170930-thumbnail.jpg?width=120&height=120&fit=bounds" /> Clinical study types and designs are terms which represent the way in which clinical trials are structured and formulated. Since we all know that clinical research is an extremely complex topic and not everything can be explained in a simple way, here we’ll focus only on some of the most basic types of clinical study types and designs which involve human subjects or participants. First of all, you should know that the most basic grouping of study designs is experimental (treatment) studies and observational studies. As we can suppose from the names, in an observational study, researchers have less control over subjects and they’re just observing what happens to subjects, while in experimental studies, researchers are using different methods (such as randomization) to place subjects in separate groups. This gives experimental studies much more validity than observational studies. In this guide, we’ll talk about the 2 possible types of studies, as well as different study designs within.

Types and Designs of Clinical Studies from Anand Butani

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0 https://public.slidesharecdn.com/v2/images/profile-picture.png https://cdn.slidesharecdn.com/ss_thumbnails/financing-investigatorpaymentmodelsbestbudgetpractices-170202200121-171114183014-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/financing-investigator-payment-models-best-budget-practices-82065832/82065832 Financing - Investigat... https://cdn.slidesharecdn.com/ss_thumbnails/ebook-gotstudies-guidetonewstudies-trialjoin-170202200529-171114182843-thumbnail.jpg?width=320&height=320&fit=bounds AnandButani/got-studies-a-quick-guide-to-help-you-get-clinical-research-studies Got Studies? A Quick G... https://cdn.slidesharecdn.com/ss_thumbnails/5reaonswehelpliftoffyourstudy-gifppt-170222192926-171114182403-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/5-reasons-we-help-lift-off-your-study-82065477/82065477 5 Reasons We Help Lift...