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Clinical research associate responsebility
This PPT give information about Institutional Human Ethics Committee
stake holders in clinical trail
Good clinical practice guidelines
institutional ethics committee
Informed consent form
An informed consent form is a document that is provided to prospective participants in a research st...
What is Investigator's Brochure? What are its importance? why it is useful? What are the content...
Embark on a comprehensive journey into the dynamic and critical realm of Clinical Research. This pre...
inform consent form before participate in clinical trials.for purpose of understanding the nature of...
ICH E 6 good clinical practice (GCP)
Regulatory writing
Investigatot brochure clinical trail
An overview of ICH-GCP guidelines of clinical trials. Good clinical practice (GCP): a standard for t...
Good Clinical Practices
baik
Informed consent is a process in which a patient or research participant is provided with informatio...
Pharmacovigilance
Investigators broucher regulatory affairs pharmacy
ICH GCP guidelines for mpharmacy 2nd sem 204T subject. topic include the brief description regarding...
Drug development , uses and it's applications, pre clinical trails
clinical trial application in india
These slides re prepared to give the basic knowledge about the planning and execution of clinical tr...