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This presentation enumerates the responsibilities of various clinical trial players whilst managing ...
Regulatory documents in clinical research
Good Laboratory Practice (GLP),Organization for Economic Co-operation and Development(OECD),National...
Good Clinical Practices
declaration of helsinki
ACL PLUS LET
Significance of bioavailability Studies Importance of bioavailability Studies Advantages bioavailabi...
spinal vs local anesthesia on hernia repair
declaration of helsinki, research methodology
Role of Ethics committee members in clinical research. Please give your suggestions if any needed.
Lecture notes for UG MBBS
The ppt gives a basic information about ICH-GCP, how it originated , what led to the formation of IC...
Randomized Controlled Trial
ON GOING
institutional review board and independent ethics committee, their composition, functions etc.
clinical research
this ppt contains basics of experimental design concepts for 2nd year mbbs students, and third year ...
21 CFR 312 and 314 are two separate, but related, US Food and Drug Administration (FDA) regulations ...
Introduction to Clinical Data Management Process Overview in Pharmaceuticals, Bio-Pharmaceuticals, M...
(Agencia Nacional de Vigilancia Sanitaria) ( Brazilian Health Surveillance Agency )
updates and techniques of regenerative endodontics
CLINICAL DATA MANGEMENT (CDM)
Global submission of IND - Regulatory affairs 1st sem M. Pharm pharmaceutics
Clinical Trials
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