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CRO
In the past few years, US FDA has implemented the concepts of Quality by Design (QbD) into its appro...
GLP, QA, QC implementation in pharmaceutical lab
validation master plan for industry
Indian GMP Certification & WHO GMP Certification by Mr. Vishal Shelke https://youtube.com/visha...
the topic documentation include their need their importance, purpose of documentation, feature of do...
Development and clinical uses of tumor markers
Investigational medicinal product dossier (IMPD) and Investigational brochure (IB) in Regulatory aff...
It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...
This presentation gives knowledge on ICH and its History, Mission, and overview of ICH Quality, Safe...
Pharmaceutical Regulataory Affairs
Activity in chemistry
Organizational structure
IMPURITIES IN NEW DRUG SUBSTANCES
This is my 44th powerpoint........deals with ICH guidelines..... Deals with brief introduction, prec...
Quality assurance
Regulatory requirements of BIOAVAILABLITY & BIOEQUIVALENCE STUDIES
ICH Guidelines were created by The International Council for Harmonization of Technical Requirements...
Validation of Packaging operations
Technology Transfer OSD
analytical chemistry.... The design feature
