Found 127 presentations matching your search
Informed consent process a prerequisite in any clinical trial study as an understanding between the...
A brief introduction to Drug Regulatory Affairs and Its Regulatory Authority.
Clinical Trials
schedule y of drugs and cosmetic acts
Pharmacological and Toxicological screening method-II, Mpharm (Pharmacology),1st year, 1st semester
Role of Ethics committee members in clinical research. Please give your suggestions if any needed.
This presentation explains the stages of drug discovery and the clinical evaluation process. It cove...
ethics committee slides by Dr Satyabrata Sahoo
institutional ethics committee
Research Methodology and Biostatistic...Declaration of Helsinki
pharmacology
Crp
This document describes the detailed information of clinical trial protocol and protocol design. The...
QAQC
5. Unit-V- Regulatory Concepts. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY ...
Basics of Clinical Data Management
Essential documents for conduct a clinical trials
Informed Consent Documents are a crucial part of clinical trials. An in depth understanding of same ...
Investigational medicinal product dossier (IMPD) and Investigational brochure (IB) in Regulatory aff...
Clinical trial and types
REGULATORY AFFAIRS FIRST SEMESTER M.PHARM
CLINICAL DATA MANGEMENT (CDM)
Basics of Clinical Research
