Found 122 presentations matching your search
GCP is a set of guidelines for how clinical trials should be carried out. It ensures that the data...
GCP guidelines for clinical research
4. Unit-IV:- Clinical Trials. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SC...
In any work or process documents that are needed before initiation, Between or generally the end of ...
This presentation is a brief overview of ICH-GCP guidelines. Although ICH-GCP is a very vast topic, ...
institutional review board and independent ethics committee, their composition, functions etc.
This presentation provides an in-depth overview of ethical considerations in biomedical and health r...
M. Pharmacy - Pharmaceutical Regulatory Affairs (MRA) 1st Semester - Clinical Research Regulations (...
From history and with case studies
ETHICS IN BIOMEDICAL RESEARCH (Clinical Research).
Investigator roles
Working on Clinical Trials – Getting started Very few clinical trials are conducted only in one c...
This slide contain information about the ethics committee.
Good Clinical Practice (GCP) guidelines are a set of international ethical and scientific standards ...
This presentation provides a comprehensive overview of Good Clinical Practice (GCP), an internationa...
regulatory affairs/Agency,IND,Types of IND, Tyes of IND application,Investigator's brochure,Cont...
What is a clinical trial protocol? Clinical research is conducted according to a plan (a protocol) o...
Investigator's bronchure & investigational medicinal product dossier (ib & impd) Nav...
clinical trial approaches with clinical trial management under ethics committee
In these slides you can get the information of clinical trials which have four phase I,II,III, IV. b...
The ppt gives a basic information about ICH-GCP, how it originated , what led to the formation of IC...
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human ...
drug regulatory affairs
