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GMP for API (ICH Q7A)
Author: Mriganka
InstitutionEast India Pharmaceutical Works Limited.

Powerpoint Presentation Downloads:   8422
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ICH , the international body on harmonization od drud standards and regulatories published the standard ICH Q7A for Good Manufacturing Practices for Pharmaceutical Bulk Drugs. This presentation can of immense use for training of middle level managers engaged in pharma industry and academia.
PPT- ASEAN GMP TRAINING MODULE SANITATION HYGIENE- Slideworld Medical Search Engines
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   3938
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PPT- ASEAN GMP TRAINING MODULE SANITATION & HYGIENE
Good Manufacturing Practices GMP, Good Laboratory Practices .
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   3779
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Was present in monkey kidney cells used to grow polio virus. Found in both Salk & Sabin Vaccines, 1955-1963. SV40 is more resistant to formaldehyde inactivation. IOM
Basic Principles of GMP
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   2979
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Bioavailability and bioequivalence in Paediatric medicine . Presenter: Jean-Marc AIACHEunique Paediatric indications for the medicinal product; the age range of pediatric
Food Safety in Meat Processing
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   1645
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Any Salmonella found is unsatisfactory . 2-3 log . 5-6 log . Marginal . 1-2 log . 4-5 log . Acceptable . 1log . 3-4 log . Good . None < 3 log . Excellent . E. coli/ cm 2
GMP Good Manufacturing Practice .
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   1328
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Design-related defects have been found in such critical products as heart valves, defibrillators, pacemakers, ventilators, patient chair lifts and laboratory tests.
Good Manufacturing Practices GMP, Good Laboratory Practices .
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   1082
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A vehicle composed of DNA (or RNA) for transferring a gene or other nucleic acid sequence of interest; frequentlyRegulations Published in the Federal Register in draft
cleaning validation
Author: ravi
InstitutionShri Bhoagwan College Of pharmacy ,Aurangabad

Powerpoint Presentation Downloads:   967
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cleaning validation is an important aspect in pharmaceutical industry to avoid cross contamination .It is regulatory requirement by GMP,WHO,cGMP.
PPT- WHO Training Workshop on Pharmaceutical Quality, GMP and ...- Slideworld Medical Search Engines
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   764
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PPT- WHO Training Workshop on Pharmaceutical Quality, GMP and ...
Ayurvedic Pharmacy Current Concepts and GMP Norms
Author: Anonymous
Institution

Powerpoint Presentation Downloads:   748
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Ayurvedic Pharmacy Current Concepts and GMP Norms
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