Sample paper(5)
Download as docx, pdf0 likes163 views
The document provides a practice exam for a Hospital Pharmacy course, including 4 short answer questions about outpatient and inpatient dispensing, types of drug distribution systems, sources of drug information, and medication errors. Students have 1 hour to answer 3 of the 4 questions worth 5 marks each for a total of 15 marks.
1 of 1
Download to read offline
Ad
Recommended
Embase: An introduction to indexing 20 October 2014
Embase: An introduction to indexing 20 October 2014Ann-Marie Roche
油
The document is a presentation by Ann-Marie Roche about indexing in Embase, aiming to educate users on its impact on search results. It details the indexing process, including the dynamic updating of drug and device terms, and highlights features like the extensive thesaurus and adverse event definitions. Additionally, it encourages interaction during the webinar and provides information on further resources and upcoming sessions.Army Public School and College Girls, Humayun Road, Rawalpindi
Army Public School and College Girls, Humayun Road, Rawalpindidfcpakistan
油
The document outlines a campaign organized by Army Public School and College in Rawalpindi aimed at promoting the idea of focusing on duties rather than rights among Pakistani citizens, particularly through student participation. The campaign includes activities like brainstorming sessions, role plays, and self-evaluation checklists to encourage behavioral change and civic responsibility. Feedback from participants indicates a significant impact on their attitudes and actions regarding societal responsibilities.Implementation of cbme curriculum in pharmacology
Implementation of cbme curriculum in pharmacologySoni Kumari
油
The document outlines plans for implementing a competency-based medical education (CBME) curriculum in pharmacology at a university. Key points include:
- The new curriculum will focus on integrated teaching, interactive methods, applied learning, and communication skills.
- 85 competencies are identified across topics in pharmacology, clinical pharmacy, clinical pharmacology, experimental pharmacology, and communication pharmacology.
- 4 competencies require certification, to be assessed through skill stations and log books.
- The curriculum incorporates vertical and horizontal integration across topics, as well as self-directed learning.
- Internal assessments will include theory, practical, and skills-based evaluations to measure competencies.
- TrainingImplementation of cbme curriculum in pharmacology
Implementation of cbme curriculum in pharmacologySoni Kumari
油
The document outlines plans for implementing a competency-based medical education (CBME) curriculum in pharmacology at a university. Key points include:
- The new curriculum will focus on integrated teaching, interactive methods, applied learning, and communication skills.
- 85 competencies are identified across topics in pharmacology, clinical pharmacy, clinical pharmacology, experimental pharmacology, and communication pharmacology.
- 4 competencies require certification, to be assessed through skill stations and log books.
- The curriculum incorporates vertical and horizontal integration across topics, as well as self-directed learning.
- Internal assessments will include theory, practical, and skills-based evaluations to measure competencies.
- FacICMR & Y.pptx experimental pharmacology pharmacy
ICMR & Y.pptx experimental pharmacology pharmacysyamjith2019
油
Schedule Y and Schedule Y 2 were established in 1988 to regulate the import and manufacture of new drugs in India, including guidelines for clinical trials and drug quality. The document outlines the data and procedures required for clinical trials, including toxicology studies and ethical considerations, aiming to align with global standards. Additionally, it details the role of the Indian Council of Medical Research (ICMR) in promoting biomedical research, including its structure, funding, and various health schemes.Worldwide comprehensive study of guideline on clinical trial
Worldwide comprehensive study of guideline on clinical trialRGPV BHOPAL
油
The document provides information on various aspects of clinical trials including:
- The different phases of clinical trials from Phase 0 to Phase V
- Key elements of a clinical trial protocol such as objectives, design, and methodology
- Regulatory requirements for conducting clinical trials including compliance with ICH GCP guidelines
- Common recruitment strategies and important documents required for clinical trial authorization applications such as the clinical trial protocol, investigator brochure, and informed consent forms.Regulatory affairs and Intellectual Property Rights
Regulatory affairs and Intellectual Property Rightssantoshnarla
油
The document provides details about Dr. Santosh Kumar Narla's academic and professional background. It states that he holds a Ph.D. in Pharmaceutical Sciences and has over 15 years of experience in formulation development and regulatory affairs. He currently works as a manager of regulatory affairs at Dr. Reddy's Laboratories in Hyderabad. It also lists his publications and presentations at national and international conferences.Embase indexing (webinar 28 oct)
Embase indexing (webinar 28 oct)Ann-Marie Roche
油
The document discusses Embase indexing. It provides an overview of how Embase indexes drugs, diseases, and medical devices in depth using subheadings, trade names, manufacturers, and CAS numbers. It also discusses other indexing features like major focus terms mapped from MEDLINE, automatic indexing using Emtree terms, check tags for limits, and indexing of study types and topic terms. The document outlines the agenda which includes a history of indexing at Embase and a focus on in-depth drug, disease, and device indexing.PharmaPendium - An Introduction.25april2012
PharmaPendium - An Introduction.25april2012Ann-Marie Roche
油
The Pharmapendium webinar introduces its platform, which offers searchable FDA approval packages and EMA EPARs with over 1.9 million pages of data for informed drug development. It focuses on preclinical, clinical, and post-marketing data, including pharmacokinetic and safety observations, using normalized terminology for searches. Participants can engage in Q&A and will receive further information via email about the next webinar and related training materials.IND SUBMISSIONS ppt Sourav Pal.pptx
IND SUBMISSIONS ppt Sourav Pal.pptxSouravPal89
油
The document discusses the investigational new drug (IND) application process, which pharmaceutical companies must follow to commence human clinical trials. It outlines the types of INDs, required contents, and regulations in the USA, Europe, India, and other countries. The document also highlights recent amendments to clinical trial regulations and emphasizes the importance of safety and ethical standards in drug development.Pmy 4030 course handbook 2014
Pmy 4030 course handbook 2014University of Zambia, School of Pharmacy, Lusaka, Zambia
油
This document provides the course syllabus for Pharmaceutics III at the University of Zambia School of Medicine Department of Pharmacy for the 2015/2016 period. The 110-hour course deals with applying physicochemical and physiological principles to the design and manufacturing of pharmaceutical dosage forms. The objectives are to describe drug delivery processes and compounding of sterile and non-sterile dosage forms, as well as evaluating manufacturing procedures. Assessment includes tests, assignments, laboratory reports. The course covers topics like drug delivery systems, non-sterile dosage forms, external drug delivery forms, and new drug systems through lectures and tutorials.Phase 3
Phase 3SwaroopaNallabariki
油
This document provides an overview of phase 3 clinical trials. Phase 3 trials involve large randomized controlled trials of up to 3000 patients to generate statistically significant data on a drug's safety and efficacy in different patient populations. The objectives are to demonstrate therapeutic efficacy and safety/tolerability in a representative sample. Results are submitted to regulatory agencies for marketing approval. Challenges include long duration, large sample sizes, high costs, and coordinating multiple study sites. If approved, the new drug application process requires submission of all safety, efficacy and manufacturing data to the regulatory agency for review and potential approval.Study_Design_PICO_etc_2023_(4) for study designs
Study_Design_PICO_etc_2023_(4) for study designsKAMRAN HANIF
油
to learn about the study designs in health Vish- Concept and Historical Development of Pharmaceutical Product Registration
Vish- Concept and Historical Development of Pharmaceutical Product RegistrationVishal Parikh
油
This document discusses the concept and historical development of pharmaceutical product registration. It provides three key points:
1) National authorities require registrants to submit data on a drug's quality, safety and efficacy for registration. This data is either subject to temporary exclusivity protection for the original applicant or can be relied upon by other companies to register similar products.
2) Extensive testing is required to register a new pharmaceutical product, including preclinical animal testing and three phases of clinical human trials to establish safety, efficacy and appropriate dosages.
3) National registration systems keep detailed records on all registered products for authorities to check registration status and progress of applications over time, transitioning from paper books to electronic systems.Mastering Evidence-Based Medicine: Knowledge Assessment Practice (Part 1)
Mastering Evidence-Based Medicine: Knowledge Assessment Practice (Part 1)Dr. Tarun Singh
油
The document discusses the principles of evidence-based medicine as critical to clinical care and research, emphasizing the importance of training, patient preferences, and the utilization of current medical literature. It highlights the necessity of physician duty to seek and apply the most accurate information for patient benefit while acknowledging possible biases in available evidence. The role of patient involvement in decision-making is also reinforced, although it may present challenges.Asthma free copy 100 mcqs
Asthma free copy 100 mcqsDennis George
油
The document discusses multiple choice questions (MCQs) related to asthma. It provides information on the composition of airways in the lungs, the function of mucosa and mast cells, and the cellular elements responsible for mediator release in asthma, including mast cells, basophils, eosinophils, neutrophils, and macrophages. It also provides the correct answers to sample MCQs testing this knowledge.Framingham Heart Study: A Review of Research Design by Urooj Tahir in Interve...
Framingham Heart Study: A Review of Research Design by Urooj Tahir in Interve...CrimsonPublishersIOD
油
The document is a comprehensive review of the Framingham Heart Study, detailing its research design and objectives related to cardiovascular disease (CVD). It covers various cohorts, including the original cohort, offspring cohort, and new offspring spouse cohort, emphasizing their roles in studying the epidemiology of coronary heart disease over generations. Key aspects such as sampling methods, informed consent processes, and advanced screening tools used in the study are also discussed.PharmaPendium - An introduction June 2012
PharmaPendium - An introduction June 2012Ann-Marie Roche
油
The Pharmapendium webinar introduces a platform that offers searchable FDA approval packages and EMA EPARs, providing access to over 1.9 million pages of historical drug development data. The tool assists in preclinical assessments and regulatory affairs by compiling safety and pharmacokinetic data, utilizing normalized terminology for effective searches. Participants were guided through the features, including a pharmacokinetic module, and invited to future webinars for further insights on pharmacokinetics.COMMON JOB INTERVIEW QUESTIONS WITH ANSWERS ASKED IN DRUG REGULATORY AFFAIRS ...
COMMON JOB INTERVIEW QUESTIONS WITH ANSWERS ASKED IN DRUG REGULATORY AFFAIRS ...Pristyn Research Solutions
油
The document provides an overview of common job interview questions and answers related to drug regulatory affairs, explaining the roles and goals of regulatory affairs professionals in the pharmaceutical industry. It details various applications like NDA, ANDA, IND, and MAA, along with definitions of key terms such as DMF, ASMF, CTD, and guidelines for submission. Additionally, it outlines important regulations such as the Hatch-Waxman Act and the procedures for drug approval both in the U.S. and Europe.Approval and Application Process involved in Investigational New Drug (IND)
Approval and Application Process involved in Investigational New Drug (IND)Nipun Gupta
油
The document outlines the stages of drug development, focusing on the investigational new drug application (IND) process, including preclinical testing and clinical research phases. It details the responsibilities of the FDA and sponsor companies, the application formats, and the distinctions between new drug applications (NDA) and abbreviated new drug applications (ANDA). The summary highlights the timeline, costs, and classifications of changes to approved applications.Clinical Solutions White Paper
Clinical Solutions White PaperMichael Passanante
油
This white paper discusses four ways that pharmaceutical and biotechnology companies can accelerate their clinical portfolio strategy using advanced analytics and clinical trial data and technology. It provides examples of how visualizing clinical trial data over time, benchmarking trial durations, mapping competitive drug pipelines, and comparing safety profiles across trials can provide insights to help with strategic decision making regarding clinical development.Drug Discovery & Development Overview
Drug Discovery & Development OverviewMikeSumner
油
The document discusses the key stages in the drug discovery and development process including target selection, compound screening and hit optimization, selecting a drug candidate through further optimization of properties like absorption and metabolism, safety testing in animals and humans, proof of concept clinical trials in patients, large phase 3 clinical trials for registration and approval, and finally launch and life cycle management. It notes that the entire process from discovery to approval can take 12-16 years and cost over $1 billion.New Drug Application(Nda) Vs Abbreviated New Drug Application (Anda)
New Drug Application(Nda) Vs Abbreviated New Drug Application (Anda)Vamsikrishna Reddy
油
The document summarizes the key differences between a New Drug Application (NDA) and an Abbreviated New Drug Application (ANDA). An NDA is required for approval of new pharmaceuticals and contains extensive nonclinical and clinical data to establish safety and effectiveness. An ANDA is for generic drugs and contains bioequivalence data comparing it to an existing approved drug, but does not require new clinical trials. The review process is shorter for ANDAs compared to NDAs. The document also discusses patent certification requirements for ANDAs and exclusivity periods for orphan drugs.INDA/NDA/ANDA
INDA/NDA/ANDARohit Bhosale
油
The document is a comprehensive overview of the processes and requirements for Investigational New Drug (IND), New Drug Application (NDA), and Abbreviated New Drug Application (ANDA) submissions to the FDA. It includes details on the types of INDs, the information required for NDA applications, review timelines, and FDA guidelines for drug approvals. The content emphasizes the significance of well-structured applications and the regulatory framework governing drug development and approval.United States Pharmacopeia USP-NF Presentationpdf
United States Pharmacopeia USP-NF Presentationpdfharshsrivastav941
油
this has knowledge about the USP-NF
about details of monographs.it consist of a specific banaba leaf monographPmy 5040 course handbook 2014
Pmy 5040 course handbook 2014University of Zambia, School of Pharmacy, Lusaka, Zambia
油
This document outlines the course syllabus for Pharmaceutics IV, a fourth year pharmacy course at the University of Zambia School of Medicine. The course aims to apply physicochemical and physiological principles to the design and manufacture of pharmaceutical dosage forms and delivery systems. It will describe drug dosage forms, clinical applications, and modern concepts involving novel dosage forms and delivery systems. Students will be assessed through tests, assignments, laboratory reports, and a final examination. Lectures will cover solid, semi-solid, liquid, and gaseous delivery systems as well as radiopharmaceutical and biotechnological systems.Dr. A. Sumathi - Molecular Pharmaceutics - Question Bank for Unit 4 & 5.pdf
Dr. A. Sumathi - Molecular Pharmaceutics - Question Bank for Unit 4 & 5.pdfSumathi Arumugam
油
The document is a question bank for an M.Pharmacy course focused on pharmaceutics, specifically targeting aerosol systems and gene delivery methods. It includes essay prompts and short note topics based on previous university exam questions, covering areas such as aerosol systems, quality control tests, intranasal and pulmonary drug delivery, and liposomal gene delivery systems. Overall, it serves as a study guide for students in the second semester of their program.guide.pdf
guide.pdfpedapudinarendra1
油
The document provides information on how a product is developed, including literature searches, sources for information on innovators and patents, and criteria for procuring active pharmaceutical ingredients (APIs). It discusses preformulation studies including stress testing APIs under various conditions like heat, humidity, acids, bases and metals. The document also covers topics like therapeutic equivalence codes, national drug codes, drug master files, exclusivity, and types of patents listed in the Orange Book.LDMMIA Practitioner Student Reiki Yoga S2 Video PDF Without Yogi Goddess
LDMMIA Practitioner Student Reiki Yoga S2 Video PDF Without Yogi GoddessLDM & Mia eStudios
油
A bonus dept update. Happy Summer 25 almost. Do Welcome or Welcome back. Our 10th Free workshop will be released the end of this week, June 20th Weekend. All Materials/updates/Workshops are timeless for future students.
Your Attendance is valued.
We hit over 5k views for Spring Workshops and Updates-TY.
Coming to our Shop This Weekend.
Timeless for Future Grad Level Students.
Practitioner Student. Level/Session 2 Packages.
* The Review & Topics:
* All virtual, adult, education students must be over 18 years to attend LDMMIA eClasses and vStudio Thx.
* Please refer to our Free Workshops anytime for review/notes.
* Orientation Counts as S1 on introduction. Sold Separately as a PDF. Our S2 includes 2 Videos within 2 Mp4s. Sold Separately for Uploading.
* Reiki Is Japanese Energy Healing used Globally.
* Yoga is over 5k years old from India. It hosts many styles, teacher versions, and its Mainstream now vs decades ago.
* Teaching Vod, 720 Res, Mp4: Yoga Therapy is Reviewed as a Hatha, Classical, Med Yoga (ND) Base. Take practice notes as needed or repeat videos.
* Fused Teaching Vod, 720 Res, Mp4: Yoga Therapy Meets Reiki Review. Take Practice notes as needed or repeat videos.
* Video, 720 Res, Mp4: Practitioner Congrats and Workshop Visual Review with Suggestions.
Bonus Studio Video, 720 Res, Mp4: Our 1st Reiki Video. Produced under Yogi Goddess, LDM Recording. As a Reiki, Kundalini, ASMR Spa, Music Visual. For Our Remastered, Beatz Single for Goddess Vevo Watchers. https://www.reverbnation.com/yogigoddess
* Our Videos are Vevo TV and promoted within the LDMMIA Profiles.
* Scheduled upload for or by Weekend Friday June 13th.
* LDMMIA Digital & Merch Shop: https://ldm-mia.creator-spring.com
* As a student, make sure you have high speed connections/wifi for attendance. This sounds basic, I know lol. But, for our video section. The High Speed and Tech is necessary. Otherwise, any device can be used. Our Zip drive files should serve MAC/PC as well.
* On TECH Emergency: I have had some rare, rough, horrid timed situations as a Remote Student. Pros and Cons to being on campus. So Any Starbucks (coffee shop) or library can be used for wifi hot spots. You can work at your own speed and pace.
* We will not be hosting deadlines, tests/exams.
* Any homework will be session practice and business planning. Nothing stressful or assignment submissions.
More Related Content
Similar to Sample paper(5) (20)
PharmaPendium - An Introduction.25april2012
PharmaPendium - An Introduction.25april2012Ann-Marie Roche
油
The Pharmapendium webinar introduces its platform, which offers searchable FDA approval packages and EMA EPARs with over 1.9 million pages of data for informed drug development. It focuses on preclinical, clinical, and post-marketing data, including pharmacokinetic and safety observations, using normalized terminology for searches. Participants can engage in Q&A and will receive further information via email about the next webinar and related training materials.IND SUBMISSIONS ppt Sourav Pal.pptx
IND SUBMISSIONS ppt Sourav Pal.pptxSouravPal89
油
The document discusses the investigational new drug (IND) application process, which pharmaceutical companies must follow to commence human clinical trials. It outlines the types of INDs, required contents, and regulations in the USA, Europe, India, and other countries. The document also highlights recent amendments to clinical trial regulations and emphasizes the importance of safety and ethical standards in drug development.Pmy 4030 course handbook 2014
Pmy 4030 course handbook 2014University of Zambia, School of Pharmacy, Lusaka, Zambia
油
This document provides the course syllabus for Pharmaceutics III at the University of Zambia School of Medicine Department of Pharmacy for the 2015/2016 period. The 110-hour course deals with applying physicochemical and physiological principles to the design and manufacturing of pharmaceutical dosage forms. The objectives are to describe drug delivery processes and compounding of sterile and non-sterile dosage forms, as well as evaluating manufacturing procedures. Assessment includes tests, assignments, laboratory reports. The course covers topics like drug delivery systems, non-sterile dosage forms, external drug delivery forms, and new drug systems through lectures and tutorials.Phase 3
Phase 3SwaroopaNallabariki
油
This document provides an overview of phase 3 clinical trials. Phase 3 trials involve large randomized controlled trials of up to 3000 patients to generate statistically significant data on a drug's safety and efficacy in different patient populations. The objectives are to demonstrate therapeutic efficacy and safety/tolerability in a representative sample. Results are submitted to regulatory agencies for marketing approval. Challenges include long duration, large sample sizes, high costs, and coordinating multiple study sites. If approved, the new drug application process requires submission of all safety, efficacy and manufacturing data to the regulatory agency for review and potential approval.Study_Design_PICO_etc_2023_(4) for study designs
Study_Design_PICO_etc_2023_(4) for study designsKAMRAN HANIF
油
to learn about the study designs in health Vish- Concept and Historical Development of Pharmaceutical Product Registration
Vish- Concept and Historical Development of Pharmaceutical Product RegistrationVishal Parikh
油
This document discusses the concept and historical development of pharmaceutical product registration. It provides three key points:
1) National authorities require registrants to submit data on a drug's quality, safety and efficacy for registration. This data is either subject to temporary exclusivity protection for the original applicant or can be relied upon by other companies to register similar products.
2) Extensive testing is required to register a new pharmaceutical product, including preclinical animal testing and three phases of clinical human trials to establish safety, efficacy and appropriate dosages.
3) National registration systems keep detailed records on all registered products for authorities to check registration status and progress of applications over time, transitioning from paper books to electronic systems.Mastering Evidence-Based Medicine: Knowledge Assessment Practice (Part 1)
Mastering Evidence-Based Medicine: Knowledge Assessment Practice (Part 1)Dr. Tarun Singh
油
The document discusses the principles of evidence-based medicine as critical to clinical care and research, emphasizing the importance of training, patient preferences, and the utilization of current medical literature. It highlights the necessity of physician duty to seek and apply the most accurate information for patient benefit while acknowledging possible biases in available evidence. The role of patient involvement in decision-making is also reinforced, although it may present challenges.Asthma free copy 100 mcqs
Asthma free copy 100 mcqsDennis George
油
The document discusses multiple choice questions (MCQs) related to asthma. It provides information on the composition of airways in the lungs, the function of mucosa and mast cells, and the cellular elements responsible for mediator release in asthma, including mast cells, basophils, eosinophils, neutrophils, and macrophages. It also provides the correct answers to sample MCQs testing this knowledge.Framingham Heart Study: A Review of Research Design by Urooj Tahir in Interve...
Framingham Heart Study: A Review of Research Design by Urooj Tahir in Interve...CrimsonPublishersIOD
油
The document is a comprehensive review of the Framingham Heart Study, detailing its research design and objectives related to cardiovascular disease (CVD). It covers various cohorts, including the original cohort, offspring cohort, and new offspring spouse cohort, emphasizing their roles in studying the epidemiology of coronary heart disease over generations. Key aspects such as sampling methods, informed consent processes, and advanced screening tools used in the study are also discussed.PharmaPendium - An introduction June 2012
PharmaPendium - An introduction June 2012Ann-Marie Roche
油
The Pharmapendium webinar introduces a platform that offers searchable FDA approval packages and EMA EPARs, providing access to over 1.9 million pages of historical drug development data. The tool assists in preclinical assessments and regulatory affairs by compiling safety and pharmacokinetic data, utilizing normalized terminology for effective searches. Participants were guided through the features, including a pharmacokinetic module, and invited to future webinars for further insights on pharmacokinetics.COMMON JOB INTERVIEW QUESTIONS WITH ANSWERS ASKED IN DRUG REGULATORY AFFAIRS ...
COMMON JOB INTERVIEW QUESTIONS WITH ANSWERS ASKED IN DRUG REGULATORY AFFAIRS ...Pristyn Research Solutions
油
The document provides an overview of common job interview questions and answers related to drug regulatory affairs, explaining the roles and goals of regulatory affairs professionals in the pharmaceutical industry. It details various applications like NDA, ANDA, IND, and MAA, along with definitions of key terms such as DMF, ASMF, CTD, and guidelines for submission. Additionally, it outlines important regulations such as the Hatch-Waxman Act and the procedures for drug approval both in the U.S. and Europe.Approval and Application Process involved in Investigational New Drug (IND)
Approval and Application Process involved in Investigational New Drug (IND)Nipun Gupta
油
The document outlines the stages of drug development, focusing on the investigational new drug application (IND) process, including preclinical testing and clinical research phases. It details the responsibilities of the FDA and sponsor companies, the application formats, and the distinctions between new drug applications (NDA) and abbreviated new drug applications (ANDA). The summary highlights the timeline, costs, and classifications of changes to approved applications.Clinical Solutions White Paper
Clinical Solutions White PaperMichael Passanante
油
This white paper discusses four ways that pharmaceutical and biotechnology companies can accelerate their clinical portfolio strategy using advanced analytics and clinical trial data and technology. It provides examples of how visualizing clinical trial data over time, benchmarking trial durations, mapping competitive drug pipelines, and comparing safety profiles across trials can provide insights to help with strategic decision making regarding clinical development.Drug Discovery & Development Overview
Drug Discovery & Development OverviewMikeSumner
油
The document discusses the key stages in the drug discovery and development process including target selection, compound screening and hit optimization, selecting a drug candidate through further optimization of properties like absorption and metabolism, safety testing in animals and humans, proof of concept clinical trials in patients, large phase 3 clinical trials for registration and approval, and finally launch and life cycle management. It notes that the entire process from discovery to approval can take 12-16 years and cost over $1 billion.New Drug Application(Nda) Vs Abbreviated New Drug Application (Anda)
New Drug Application(Nda) Vs Abbreviated New Drug Application (Anda)Vamsikrishna Reddy
油
The document summarizes the key differences between a New Drug Application (NDA) and an Abbreviated New Drug Application (ANDA). An NDA is required for approval of new pharmaceuticals and contains extensive nonclinical and clinical data to establish safety and effectiveness. An ANDA is for generic drugs and contains bioequivalence data comparing it to an existing approved drug, but does not require new clinical trials. The review process is shorter for ANDAs compared to NDAs. The document also discusses patent certification requirements for ANDAs and exclusivity periods for orphan drugs.INDA/NDA/ANDA
INDA/NDA/ANDARohit Bhosale
油
The document is a comprehensive overview of the processes and requirements for Investigational New Drug (IND), New Drug Application (NDA), and Abbreviated New Drug Application (ANDA) submissions to the FDA. It includes details on the types of INDs, the information required for NDA applications, review timelines, and FDA guidelines for drug approvals. The content emphasizes the significance of well-structured applications and the regulatory framework governing drug development and approval.United States Pharmacopeia USP-NF Presentationpdf
United States Pharmacopeia USP-NF Presentationpdfharshsrivastav941
油
this has knowledge about the USP-NF
about details of monographs.it consist of a specific banaba leaf monographPmy 5040 course handbook 2014
Pmy 5040 course handbook 2014University of Zambia, School of Pharmacy, Lusaka, Zambia
油
This document outlines the course syllabus for Pharmaceutics IV, a fourth year pharmacy course at the University of Zambia School of Medicine. The course aims to apply physicochemical and physiological principles to the design and manufacture of pharmaceutical dosage forms and delivery systems. It will describe drug dosage forms, clinical applications, and modern concepts involving novel dosage forms and delivery systems. Students will be assessed through tests, assignments, laboratory reports, and a final examination. Lectures will cover solid, semi-solid, liquid, and gaseous delivery systems as well as radiopharmaceutical and biotechnological systems.Dr. A. Sumathi - Molecular Pharmaceutics - Question Bank for Unit 4 & 5.pdf
Dr. A. Sumathi - Molecular Pharmaceutics - Question Bank for Unit 4 & 5.pdfSumathi Arumugam
油
The document is a question bank for an M.Pharmacy course focused on pharmaceutics, specifically targeting aerosol systems and gene delivery methods. It includes essay prompts and short note topics based on previous university exam questions, covering areas such as aerosol systems, quality control tests, intranasal and pulmonary drug delivery, and liposomal gene delivery systems. Overall, it serves as a study guide for students in the second semester of their program.guide.pdf
guide.pdfpedapudinarendra1
油
The document provides information on how a product is developed, including literature searches, sources for information on innovators and patents, and criteria for procuring active pharmaceutical ingredients (APIs). It discusses preformulation studies including stress testing APIs under various conditions like heat, humidity, acids, bases and metals. The document also covers topics like therapeutic equivalence codes, national drug codes, drug master files, exclusivity, and types of patents listed in the Orange Book.Framingham Heart Study: A Review of Research Design by Urooj Tahir in Interve...
Framingham Heart Study: A Review of Research Design by Urooj Tahir in Interve...CrimsonPublishersIOD
油
COMMON JOB INTERVIEW QUESTIONS WITH ANSWERS ASKED IN DRUG REGULATORY AFFAIRS ...
COMMON JOB INTERVIEW QUESTIONS WITH ANSWERS ASKED IN DRUG REGULATORY AFFAIRS ...Pristyn Research Solutions
油
Recently uploaded (20)
LDMMIA Practitioner Student Reiki Yoga S2 Video PDF Without Yogi Goddess
LDMMIA Practitioner Student Reiki Yoga S2 Video PDF Without Yogi GoddessLDM & Mia eStudios
油
A bonus dept update. Happy Summer 25 almost. Do Welcome or Welcome back. Our 10th Free workshop will be released the end of this week, June 20th Weekend. All Materials/updates/Workshops are timeless for future students.
Your Attendance is valued.
We hit over 5k views for Spring Workshops and Updates-TY.
Coming to our Shop This Weekend.
Timeless for Future Grad Level Students.
Practitioner Student. Level/Session 2 Packages.
* The Review & Topics:
* All virtual, adult, education students must be over 18 years to attend LDMMIA eClasses and vStudio Thx.
* Please refer to our Free Workshops anytime for review/notes.
* Orientation Counts as S1 on introduction. Sold Separately as a PDF. Our S2 includes 2 Videos within 2 Mp4s. Sold Separately for Uploading.
* Reiki Is Japanese Energy Healing used Globally.
* Yoga is over 5k years old from India. It hosts many styles, teacher versions, and its Mainstream now vs decades ago.
* Teaching Vod, 720 Res, Mp4: Yoga Therapy is Reviewed as a Hatha, Classical, Med Yoga (ND) Base. Take practice notes as needed or repeat videos.
* Fused Teaching Vod, 720 Res, Mp4: Yoga Therapy Meets Reiki Review. Take Practice notes as needed or repeat videos.
* Video, 720 Res, Mp4: Practitioner Congrats and Workshop Visual Review with Suggestions.
Bonus Studio Video, 720 Res, Mp4: Our 1st Reiki Video. Produced under Yogi Goddess, LDM Recording. As a Reiki, Kundalini, ASMR Spa, Music Visual. For Our Remastered, Beatz Single for Goddess Vevo Watchers. https://www.reverbnation.com/yogigoddess
* Our Videos are Vevo TV and promoted within the LDMMIA Profiles.
* Scheduled upload for or by Weekend Friday June 13th.
* LDMMIA Digital & Merch Shop: https://ldm-mia.creator-spring.com
* As a student, make sure you have high speed connections/wifi for attendance. This sounds basic, I know lol. But, for our video section. The High Speed and Tech is necessary. Otherwise, any device can be used. Our Zip drive files should serve MAC/PC as well.
* On TECH Emergency: I have had some rare, rough, horrid timed situations as a Remote Student. Pros and Cons to being on campus. So Any Starbucks (coffee shop) or library can be used for wifi hot spots. You can work at your own speed and pace.
* We will not be hosting deadlines, tests/exams.
* Any homework will be session practice and business planning. Nothing stressful or assignment submissions.
Revista digital preescolar en transformaci坦n
Revista digital preescolar en transformaci坦nguerragallardo26
油
EVOLUCIN DEL CONTENIDO DE LA EVALUACIN DE LOS RECURSOS Y DE LA FORMACIN DE LOS DOCENTESPaper 108 | Thoreaus Influence on Gandhi: The Evolution of Civil Disobedience
Paper 108 | Thoreaus Influence on Gandhi: The Evolution of Civil DisobedienceRajdeep Bavaliya
油
Dive into the powerful journey from Thoreaus 19thcentury essay to Gandhis mass movement, and discover how one mans moral stand became the backbone of nonviolent resistance worldwide. Learn how conscience met strategy to spark revolutions, and why their legacy still inspires todays social justice warriors. Uncover the evolution of civil disobedience. Dont forget to like, share, and follow for more deep dives into the ideas that changed the world.
M.A. Sem - 2 | Presentation
Presentation Season - 2
Paper - 108: The American Literature
Submitted Date: April 2, 2025
Paper Name: The American Literature
Topic: Thoreaus Influence on Gandhi: The Evolution of Civil Disobedience
[Please copy the link and paste it into any web browser to access the content.]
Video Link: https://youtu.be/HXeq6utg7iQ
For a more in-depth discussion of this presentation, please visit the full blog post at the following link: https://rajdeepbavaliya2.blogspot.com/2025/04/thoreau-s-influence-on-gandhi-the-evolution-of-civil-disobedience.html
Please visit this blog to explore additional presentations from this season:
Hashtags:
#CivilDisobedience #ThoreauToGandhi #NonviolentResistance #Satyagraha #Transcendentalism #SocialJustice #HistoryUncovered #GandhiLegacy #ThoreauInfluence #PeacefulProtest
Keyword Tags:
civil disobedience, Thoreau, Gandhi, Satyagraha, nonviolent protest, transcendentalism, moral resistance, Gandhi Thoreau connection, social change, political philosophyHow to Implement Least Package Removal Strategy in Odoo 18 Inventory
How to Implement Least Package Removal Strategy in Odoo 18 InventoryCeline George
油
In Odoo, the least package removal strategy is a feature designed to optimize inventory management by minimizing the number of packages open to fulfill the orders. This strategy is particularly useful for the business that deals with products packages in various quantities such as boxes, cartons or palettes. University of Ghana Cracks Down on Misconduct: Over 100 Students Sanctioned
University of Ghana Cracks Down on Misconduct: Over 100 Students SanctionedKweku Zurek
油
University of Ghana Cracks Down on Misconduct: Over 100 Students Sanctioned
Overview of Employee in Odoo 18 - Odoo 際際滷s
Overview of Employee in Odoo 18 - Odoo 際際滷sCeline George
油
The employee module is a core component of the HR workspace that helps the business to get the employee activities and details. This would also allow you to get the employee details by acting as a centralized system and accessing, updating, and managing all the other employee data. LAZY SUNDAY QUIZ "A GENERAL QUIZ" JUNE 2025 SMC QUIZ CLUB, SILCHAR MEDICAL CO...
LAZY SUNDAY QUIZ "A GENERAL QUIZ" JUNE 2025 SMC QUIZ CLUB, SILCHAR MEDICAL CO...Ultimatewinner0342
油
Lazy Sunday Quiz | General Knowledge Trivia by SMC Quiz Club Silchar Medical College
Presenting the Lazy Sunday Quiz, a fun and thought-provoking general knowledge quiz created by the SMC Quiz Club of Silchar Medical College & Hospital (SMCH). This quiz is designed for casual learners, quiz enthusiasts, and competitive teams looking for a diverse, engaging set of questions with clean visuals and smart clues.
ｯ What is the Lazy Sunday Quiz?
The Lazy Sunday Quiz is a light-hearted yet intellectually rewarding quiz session held under the SMC Quiz Club banner. Its a general quiz covering a mix of current affairs, pop culture, history, India, sports, medicine, science, and more.
Whether youre hosting a quiz event, preparing a session for students, or just looking for quality trivia to enjoy with friends, this PowerPoint deck is perfect for you.
Quiz Format & Structure
Total Questions: ~50
Types: MCQs, one-liners, image-based, visual connects, lateral thinking
Rounds: Warm-up, Main Quiz, Visual Round, Connects (optional bonus)
Design: Simple, clear slides with answer explanations included
Tools Needed: Just a projector or screen ready to use!
Who Is It For?
College quiz clubs
School or medical students
Teachers or faculty for classroom engagement
Event organizers needing quiz content
Quizzers preparing for competitions
Freelancers building quiz portfolios
Why Use This Quiz?
Ready-made, high-quality content
Curated with lateral thinking and storytelling in mind
Covers both academic and pop culture topics
Designed by a quizzer with real event experience
Usable in inter-college fests, informal quizzes, or Sunday brain workouts
About the Creators
This quiz has been created by Rana Mayank Pratap, an MBBS student and quizmaster at SMC Quiz Club, Silchar Medical College. The club aims to promote a culture of curiosity and smart thinking through weekly and monthly quiz events.
SEO Tags:
quiz, general knowledge quiz, trivia quiz, 際際滷Share quiz, college quiz, fun quiz, medical college quiz, India quiz, pop culture quiz, visual quiz, MCQ quiz, connect quiz, science quiz, current affairs quiz, SMC Quiz Club, Silchar Medical College
Reuse & Credit
Youre free to use or adapt this quiz for your own events or sessions with credit to:
SMC Quiz Club Silchar Medical College & Hospital
Curated by: Rana Mayank PratapRay Dalio How Countries go Broke the Big Cycle
Ray Dalio How Countries go Broke the Big CycleDadang Solihin
油
A complete and practical understanding of the Big Debt Cycle. A much more practical understanding of how supply and demand really work compared to the conventional economic thinking. A complete and practical understanding of the Overall Big Cycle, which is driven by the Big Debt Cycle and the other major cycles, including the big political cycle within countries that changes political orders and the big geopolitical cycle that changes world orders.LDMMIA Practitioner Level Orientation Updates
LDMMIA Practitioner Level Orientation UpdatesLDM & Mia eStudios
油
See our 2 Starter PDFs within a Compressed, Zip Drive. Within Shop. Videos will be available Before the Weekend of 6/14th. For the US, Happy Fathers Day Weekend. (Our readers/teams are global.) Also, our content remains timeless for Future Grad Students seeking updates.
After about a Year or 10, I retire older content. Literally up to under 10 yrs. We will be 19 yrs old this Aug for Love and Divinity in Motion (LDM). How old are we? So funny. Our oldest profile is X, formerly Twitter. From our old Apple Podcast Years.
https://ldm-mia.creator-spring.com
Session/Lesson 1 -Intro
REIKI- YOGA ORIENTATION
It helps to understand the text behind anything. This improves our performance and confidence.
Your training will be mixed media. Includes Rehab Intro and Meditation vods, all sold separately.
Editing our Vods & New Shop. Retail under $30 per item.
*Store Fees will apply. *Digital Should be low cost.
Thank you for attending our free workshops. Those can be used with any Reiki Yoga training package. Traditional Reiki does host rules and ethics. Its silent and within the JP Culture/Area/Training/Word of Mouth. It allows remote healing but theres limits for practitioners and masters. We are not allowed to share certain secrets/tools. Some content is designed only for Masters...
Next Upload will be our Video package for Session 1. Prices will be affordable as possible. Thx for becoming a "Practitioner Level" Student.
Updates so far, are every week for spring. Summer should be a similar schedule. Thx for visitings, attending, and following LDMMIA.
Social Media:
https://x.com/OnlineDrLeZ
and
https://www.instagram.com/chelleofsl/
Communicable Diseases and National Health Programs Unit 9 | B.Sc Nursing 5t...
Communicable Diseases and National Health Programs Unit 9 | B.Sc Nursing 5t...RAKESH SAJJAN
油
This PowerPoint presentation covers Unit 9 Communicable Diseases and National Health Programs, a core part of the 5th Semester B.Sc Nursing (Community Health Nursing I) syllabus, as outlined by the Indian Nursing Council (INC).
This unit enables nursing students to understand the epidemiology, prevention, control, and nursing management of common communicable diseases in India, while also offering a structured overview of the National Health Programs implemented to address them.
The content is critical for effective field practice, disease surveillance, early detection, referral, and health education, equipping students to participate in public health interventions and outbreak control at community and national levels.
Key Topics Covered in the PPT:
Definition and classification of communicable diseases
Modes of transmission and chain of infection
Common communicable diseases in India:
Malaria
Tuberculosis
Leprosy
Dengue
HIV/AIDS
Hepatitis
COVID-19 (if included in the current curriculum)
Diarrheal diseases
Acute Respiratory Infections (ARIs)
Epidemiological factors, causative agents, symptoms, and incubation periods
Prevention and control strategies: primary, secondary, and tertiary levels
Nursing responsibilities in patient care, contact tracing, community surveillance, and outbreak control
Health education and behavior change communication for community awareness
Vaccination schedules and cold chain maintenance
National Health Programs related to communicable diseases:
National Vector Borne Disease Control Program (NVBDCP)
Revised National Tuberculosis Control Program (RNTCP)
National Leprosy Eradication Program (NLEP)
National AIDS Control Program (NACP)
Universal Immunization Program (UIP)
IDSP Integrated Disease Surveillance Program
Overview of standard treatment protocols, referral mechanisms, and community nurses role in program implementation
This presentation is ideal for:
Nursing students preparing for university exams, class tests, and field projects
Tutors teaching infectious disease nursing and public health interventions
Nurses involved in immunization, outbreak investigation, and contact tracing
It provides a student-friendly breakdown of concepts, aligned with national priorities, including flowcharts, tables, case examples, and simplified text for field-level application.Publishing Your Memoir with Brooke Warner
Publishing Your Memoir with Brooke WarnerBrooke Warner
油
Brooke Warner presents on getting published - traditional, hybrid, and self-publishing.
www.memoirnation.comIntroduction to Generative AI and Copilot.pdf
Introduction to Generative AI and Copilot.pdfTechSoup
油
In this engaging and insightful two-part webinar series, where we will dive into the essentials of generative AI, address key AI concerns, and demonstrate how nonprofits can benefit from using Microsofts AI assistant, Copilot, to achieve their goals.
This event series to help nonprofits obtain Copilot skills is made possible by generous support from Microsoft.Non-Communicable Diseases and National Health Programs Unit 10 | B.Sc Nursi...
Non-Communicable Diseases and National Health Programs Unit 10 | B.Sc Nursi...RAKESH SAJJAN
油
This PowerPoint presentation is prepared for Unit 10 Non-Communicable Diseases and National Health Programs, as per the 5th Semester B.Sc Nursing syllabus outlined by the Indian Nursing Council (INC) under the subject Community Health Nursing I.
This unit focuses on equipping students with knowledge of the causes, prevention, and control of non-communicable diseases (NCDs), which are a major public health challenge in India. The presentation emphasizes the nurses role in early detection, screening, management, and referral services under national-level programs.
Key Topics Included:
Definition, burden, and impact of NCDs in India
Epidemiology, risk factors, signs/symptoms, prevention, and management of:
Diabetes Mellitus
Hypertension
Cardiovascular Diseases
Stroke & Obesity
Thyroid Disorders
Blindness
Deafness
Injuries and Accidents (incl. road traffic injuries and trauma guidelines)
NCD-2 Cancers:
Breast Cancer
Cervical Cancer
Oral Cancer
Risk factors, screening, diagnosis, early signs, referral & palliative care
Role of nurse in screening, referral, counseling, and continuum of care
National Programs:
National Program for Prevention and Control of Cancer, Diabetes, Cardiovascular Diseases and Stroke (NPCDCS)
National Program for Control of Blindness
National Program for Prevention and Control of Deafness
National Tobacco Control Program (NTCP)
Introduction to Universal Health Coverage and Ayushman Bharat
Use of standard treatment protocols and referral flowcharts
This presentation is ideal for:
Classroom lectures, field assignments, health education planning, and student projects
Preparing for university exams, class tests, and community field postingsECONOMICS, DISASTER MANAGEMENT, ROAD SAFETY - STUDY MATERIAL [10TH]
ECONOMICS, DISASTER MANAGEMENT, ROAD SAFETY - STUDY MATERIAL [10TH]SHERAZ AHMAD LONE
油
This study material for Class 10th covers the core subjects of Economics, Disaster Management, and Road Safety Education, developed strictly in line with the JKBOSE textbook. It presents the content in a simplified, structured, and student-friendly format, ensuring clarity in concepts. The material includes reframed explanations, flowcharts, infographics, and key point summaries to support better understanding and retention. Designed for classroom teaching and exam preparation, it aims to enhance comprehension, critical thinking, and practical awareness among students.Health Care Planning and Organization of Health Care at Various Levels Unit...
Health Care Planning and Organization of Health Care at Various Levels Unit...RAKESH SAJJAN
油
This comprehensive PowerPoint presentation is prepared for B.Sc Nursing 5th Semester students and covers Unit 2 of Community Health Nursing I based on the Indian Nursing Council (INC) syllabus. The unit focuses on the planning, structure, and functioning of health care services at various levels in India. It is especially useful for nursing educators and students preparing for university exams, internal assessments, or professional teaching assignments.
The content of this presentation includes:
Historical development of health planning in India
Detailed study of various health committees: Bhore, Mudaliar, Kartar Singh, Shrivastava Committee, etc.
Overview of major health commissions
In-depth understanding of Five-Year Plans and their impact on health care
Community participation and stakeholder involvement in health care planning
Structure of health care delivery system at central, state, district, and peripheral levels
Concepts and implementation of Primary Health Care (PHC) and Sustainable Development Goals (SDGs)
Introduction to Comprehensive Primary Health Care (CPHC) and Health and Wellness Centers (HWCs)
Expanded role of Mid-Level Health Providers (MLHPs) and Community Health Providers (CHPs)
Explanation of national health policies: NHP 1983, 2002, and 2017
Key national missions and schemes including:
National Health Mission (NHM)
National Rural Health Mission (NRHM)
National Urban Health Mission (NUHM)
Ayushman Bharat Pradhan Mantri Jan Arogya Yojana (PM-JAY)
Universal Health Coverage (UHC) and Indias commitment to equitable health care
This presentation is ideal for:
Nursing students (B.Sc, GNM, Post Basic)
Nursing tutors and faculty
Health educators
Competitive exam aspirants in nursing and public health
It is organized in a clear, point-wise format with relevant terminologies and a focus on applied knowledge. The slides can also be used for community health demonstrations, teaching sessions, and revision guides.Q1_ENGLISH_PPT_WEEK 1 power point grade 3 Quarter 1 week 1
Q1_ENGLISH_PPT_WEEK 1 power point grade 3 Quarter 1 week 1jutaydeonne
油
Grade 3 Quarter 1 Week 1 English part 2Chalukyas of Gujrat, Solanki Dynasty NEP.pptx
Chalukyas of Gujrat, Solanki Dynasty NEP.pptxDr. Ravi Shankar Arya Mahila P. G. College, Banaras Hindu University, Varanasi, India.
油
This presentation has been made keeping in mind the students of undergraduate and postgraduate level. In this slide try to present the brief history of Chaulukyas of Gujrat up to Kumarpala To keep the facts in a natural form and to display the material in more detail, the help of various books, websites and online medium has been taken. Whatever medium the material or facts have been taken from, an attempt has been made by the presenter to give their reference at the end.
Chaulukya or Solanki was one of the Rajputs born from Agnikul. In the Vadnagar inscription, the origin of this dynasty is told from Brahma's Chauluk or Kamandalu. They ruled in Gujarat from the latter half of the tenth century to the beginning of the thirteenth century. Their capital was in Anahilwad. It is not certain whether it had any relation with the Chalukya dynasty of the south or not. It is worth mentioning that the name of the dynasty of the south was 'Chaluky' while the dynasty of Gujarat has been called 'Chaulukya'. The rulers of this dynasty were the supporters and patrons of Jainism.Chalukyas of Gujrat, Solanki Dynasty NEP.pptx
Chalukyas of Gujrat, Solanki Dynasty NEP.pptxDr. Ravi Shankar Arya Mahila P. G. College, Banaras Hindu University, Varanasi, India.
油
Ad
Sample paper(5)
- 1. HIMT COLLEGE OF PHARMACY, GR. NOIDA 3rd Sessional Examination (Theory) 2014-15 Semester VII Subject name & Code- Hospital Pharmacy (Pharm-484) Max Marks 15 Duration: 1 Hour Attempt any three questions: Q.1 Describe out-patient and in-patient dispensing. (5) Q.2 Enlist various types of drug distribution system. (5) Q.3. Write a short note on Sources of information on drugs. (5) Q.4 Write a short note Medication Error. (5) HIMT COLLEGE OF PHARMACY, GR. NOIDA 3rd Sessional Examination (Theory) 2014-15 Semester VII Subject name & Code- Hospital Pharmacy (Pharm-484) Max Marks 15 Duration: 1 Hour Attempt any three questions: Q.1 Describe out-patient and in-patient dispensing. (5) Q.2 Enlist various types of drug distribution system. (5) Q.3. Write a short note on Sources of information on drugs. (5) Q.4 Write a short note Medication Error. (5)