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Brief ppt on evaluation of TDDSs with diagrammatic representation & recent research reports.
Concepts of GLP and ISO 9000. The Good Laboratory Practices Guideline (GLP) is an FDA regulation. Go...
ICH
Market Research is the process of designing , collecting, analysing and reporting information that m...
5. Unit-V- Regulatory Concepts. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY ...
It's all about the topic of documentation in pharmaceutical industry. In this the specifications...
The New Drugs and Clinical Trials Rules, 2019 (NDCT Rules, 2019) apply to all new drugs, investigati...
HOW TO CRITICALLY APPRAISE A DPL
COMPLAINT HANDLING IN PHARMACEUTICAL COMPANIES,�PRODUCT RECALL,RETENTION RECORDS, DISTRIBUTION RE...
In this webinar we introduce you to the workflows supported by Embase, describe the benefits of Emba...
Basics of Clinical Research
Pharmaceutical Quality Assurance B.Pharmacy Third Year Sem- VI As Per PCI syllabus
OECD Guidelines for conducting Acute oral toxicity TGs No 423 (Acute toxic class method)
Product Development & Technology Transfer
Pharmacovigilance
B PHARMA 6TH SEM PHRAMACEUTICAL QUALITY ASSURANCE Pharmaceutical documentation Need of documentati...
Sidha medicine
It deals with the understanding and process for auditing pharmaceutical industries. This covers the...
generic vs branded a comparison for the benefit of the society
“Clinical pharmacy is a health science discipline in which pharmacists are involved in direct pati...
pharmaceutics
Quality Risk management in pharmaceutical Industry. A general Review on Risk analysis and Risk asses...
