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13 ICH GCP guidelines
An overview of ICH-GCP guidelines of clinical trials. Good clinical practice (GCP): a standard for t...
Introduction Historical background Sections Principles Ethics committee Responsi...
The ppt gives a basic information about ICH-GCP, how it originated , what led to the formation of IC...
ICH GCP guidelines
M. Pharmacy - Pharmaceutical Regulatory Affairs (MRA) 1st Semester - Clinical Research Regulations (...
ICH GCP guidelines for mpharmacy 2nd sem 204T subject. topic include the brief description regarding...
This presentation is a brief overview of ICH-GCP guidelines. Although ICH-GCP is a very vast topic, ...
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human ...
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 Perspectives of Clinical Trials: Origin and Principles of International Conference on Har...
The complexity of a clinical research trial involves keeping and storing multiple essential document...
The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clin...
Good clinical practices-drug discovery
This SlideShare presentation provides a comprehensive exploration of Good Clinical Practice (GCP) as...
GCP guidelines for clinical research
GCP is a set of guidelines for how clinical trials should be carried out. It ensures that the data...
Good Clinical Practices and Investigator responsibilities
Good clinical practice ICH GCP E6
Regulatory perspective of clinical trials, phases of clinical trials,ICH-GCP Principles
Good Clinical Practices for drug discovery and development
Slides prepared for IIUM GCP Workshop