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Role of Ethics committee members in clinical research. Please give your suggestions if any needed.
Digit HF trial review presentation by a resident
#pharmacognosy #drsiddhiupadhyay #sigmainstituteofpharmacy
Schedule y
Clinical Trials
A brief introduction to Drug Regulatory Affairs and Its Regulatory Authority.
regulatory affairs
schedule y of drugs and cosmetic acts
Definition. A clinical research protocol is a document that describes the background, rationale, obj...
This presentation explains the stages of drug discovery and the clinical evaluation process. It cove...
ethics committee slides by Dr Satyabrata Sahoo
5. Unit-V- Regulatory Concepts. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY ...
Basics of Clinical Data Management
Pharmacological and Toxicological screening method-II, Mpharm (Pharmacology),1st year, 1st semester
Essential documents for conduct a clinical trials
clinical trials history and types
The Quick explanation on investigators brochure used in Clinical Trial/Research by the principal inv...
Investigational medicinal product dossier (IMPD) and Investigational brochure (IB) in Regulatory aff...
You can find phase II case study related to development of clinical trial protocol.
Informed Consent Documents are a crucial part of clinical trials. An in depth understanding of same ...
Research Methodology and Biostatistic...Declaration of Helsinki
REGULATORY AFFAIRS FIRST SEMESTER M.PHARM
CLINICAL DATA MANGEMENT (CDM)