狠狠撸shows by User: ICHApps / http://www.slideshare.net/images/logo.gif 狠狠撸shows by User: ICHApps / Tue, 06 Oct 2015 10:34:12 GMT 狠狠撸Share feed for 狠狠撸shows by User: ICHApps Water system , IMPORTANCE OF WATER & Water Treatment /slideshow/water-system-importance-of-water-water-treatment/53591127 watersystemppt-151006103413-lva1-app6891
Water system, IMPORTANCE OF WATER.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.]]>

Water system, IMPORTANCE OF WATER.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.]]>
Tue, 06 Oct 2015 10:34:12 GMT /slideshow/water-system-importance-of-water-water-treatment/53591127 ICHApps@slideshare.net(ICHApps) Water system , IMPORTANCE OF WATER & Water Treatment ICHApps Water system, IMPORTANCE OF WATER.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/watersystemppt-151006103413-lva1-app6891-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Water system, IMPORTANCE OF WATER.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.Water is widely used as a raw material, ingredient and solvent in the processing formulation and in the manufacture of pharmaceutical products, Active pharmaceutical ingredients and in intermediates.
Water system , IMPORTANCE OF WATER & Water Treatment from ICHAPPS
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Qualification & Validation /slideshow/qualification-validation/53588883 qualificationvalidation-151006094016-lva1-app6892
QUALIFICATION & VALIDATION.Validation is an essential part of GMP, and an element of QA.Critical steps in the process need to be validated.Need for confidence that the product will consistently meet predetermined specifications and attributes. ]]>

QUALIFICATION & VALIDATION.Validation is an essential part of GMP, and an element of QA.Critical steps in the process need to be validated.Need for confidence that the product will consistently meet predetermined specifications and attributes. ]]>
Tue, 06 Oct 2015 09:40:16 GMT /slideshow/qualification-validation/53588883 ICHApps@slideshare.net(ICHApps) Qualification & Validation ICHApps QUALIFICATION & VALIDATION.Validation is an essential part of GMP, and an element of QA.Critical steps in the process need to be validated.Need for confidence that the product will consistently meet predetermined specifications and attributes. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/qualificationvalidation-151006094016-lva1-app6892-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> QUALIFICATION &amp; VALIDATION.Validation is an essential part of GMP, and an element of QA.Critical steps in the process need to be validated.Need for confidence that the product will consistently meet predetermined specifications and attributes.
Qualification & Validation from ICHAPPS
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1 documents & Requirements /slideshow/1-documents-requirements/53588237 1documentsrequirements-151006092207-lva1-app6891
ICH Q7A GMP Guidance For API .Good Documentation Practices.Why Documentation is required..? To define the method and control. GOOD DOCUMENTATION PRACTICE ]]>

ICH Q7A GMP Guidance For API .Good Documentation Practices.Why Documentation is required..? To define the method and control. GOOD DOCUMENTATION PRACTICE ]]>
Tue, 06 Oct 2015 09:22:07 GMT /slideshow/1-documents-requirements/53588237 ICHApps@slideshare.net(ICHApps) 1 documents & Requirements ICHApps ICH Q7A 锟紾MP Guidance For API .Good Documentation Practices.Why Documentation is required..? To define the method and control. GOOD DOCUMENTATION PRACTICE <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/1documentsrequirements-151006092207-lva1-app6891-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> ICH Q7A 锟紾MP Guidance For API .Good Documentation Practices.Why Documentation is required..? To define the method and control. GOOD DOCUMENTATION PRACTICE
1 documents & Requirements from ICHAPPS
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21 CFR-FOOD AND DRUG ADMINISTRATION,锟� DEPARTMENT OF HEALTH AND HUMAN SERVICES锟�- UNITED STATES OF AMERICA /slideshow/21-cfrfood-and-drug-administration-department-of-health-and-human-services-united-states-of-america/53091792 21cfr-150923031752-lva1-app6892
TRAINING PROGRAMME ON 21CFR PARTS-210 AND 211 QUALITY ASSURANCE 狠狠撸show About 21 CFR 鈥淓very product must be fit for its intended purpose鈥� 鈥淓very product must be fit for its intended purpose鈥� FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES- UNITED STATES OF AMERICA ]]>

TRAINING PROGRAMME ON 21CFR PARTS-210 AND 211 QUALITY ASSURANCE 狠狠撸show About 21 CFR 鈥淓very product must be fit for its intended purpose鈥� 鈥淓very product must be fit for its intended purpose鈥� FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES- UNITED STATES OF AMERICA ]]>
Wed, 23 Sep 2015 03:17:52 GMT /slideshow/21-cfrfood-and-drug-administration-department-of-health-and-human-services-united-states-of-america/53091792 ICHApps@slideshare.net(ICHApps) 21 CFR-FOOD AND DRUG ADMINISTRATION,锟� DEPARTMENT OF HEALTH AND HUMAN SERVICES锟�- UNITED STATES OF AMERICA ICHApps TRAINING PROGRAMME ON 锟� 21CFR PARTS-210 AND 211 锟� QUALITY ASSURANCE 狠狠撸show About 21 CFR 鈥淓very product must be fit for its intended purpose鈥� 鈥淓very product must be fit for its intended purpose鈥� FOOD AND DRUG ADMINISTRATION,锟� DEPARTMENT OF HEALTH AND HUMAN SERVICES锟�- UNITED STATES OF AMERICA <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/21cfr-150923031752-lva1-app6892-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> TRAINING PROGRAMME ON 锟� 21CFR PARTS-210 AND 211 锟� QUALITY ASSURANCE 狠狠撸show About 21 CFR 鈥淓very product must be fit for its intended purpose鈥� 鈥淓very product must be fit for its intended purpose鈥� FOOD AND DRUG ADMINISTRATION,锟� DEPARTMENT OF HEALTH AND HUMAN SERVICES锟�- UNITED STATES OF AMERICA
21 CFR-FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES - UNITED STATES OF AMERICA from ICHAPPS
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Setting spec limit for imps /slideshow/setting-spec-limit-for-imps/52976318 settingspeclimitforimps-150920043704-lva1-app6892
Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚). Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚) Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚)]]>

Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚). Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚) Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚)]]>
Sun, 20 Sep 2015 04:37:04 GMT /slideshow/setting-spec-limit-for-imps/52976318 ICHApps@slideshare.net(ICHApps) Setting spec limit for imps ICHApps Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚). Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚) Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚) <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/settingspeclimitforimps-150920043704-lva1-app6892-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚). Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚) Setting Specification Limits for Impurities in Active Pharmaceutical Ingredient (API鈥檚)
Setting spec limit for imps from ICHAPPS
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https://cdn.slidesharecdn.com/profile-photo-ICHApps-48x48.jpg?cb=1572075322 OUR VISION: To provide the support to reduce the expenditure and time incurred by Health care and Pharma industry to resolve the regular issues like documentation, audit readiness, cGMP compliance, Risk based approaches to product and process related issues, qualifications, validations, marketing, regulatory and other requirements of health care and pharmaceutical industry world wide. www.ichapps.com https://cdn.slidesharecdn.com/ss_thumbnails/watersystemppt-151006103413-lva1-app6891-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/water-system-importance-of-water-water-treatment/53591127 Water system , IMPORTA... https://cdn.slidesharecdn.com/ss_thumbnails/qualificationvalidation-151006094016-lva1-app6892-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/qualification-validation/53588883 Qualification &amp; Valida... https://cdn.slidesharecdn.com/ss_thumbnails/1documentsrequirements-151006092207-lva1-app6891-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/1-documents-requirements/53588237 1 documents &amp; Requirem...