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Randomized Controlled Trials / RCT
bioequivalence studies biopharm -advanced biopharmaceutics
Clinical Trial Protocals, Composition of Institutional Ethical Committie, IRB, their functins
Path ppt
schedule y
This SlideShare presentation provides a comprehensive exploration of Good Clinical Practice (GCP) as...
In recent years, transcranial magnetic stimulation (TMS) has gained significant recognition as a non...
Clinical research is fundamental to advancing medical knowledge and developing new treatments. Howev...
Informed consent is a process in which a patient or research participant is provided with informatio...
This slide contain information about the ethics committee.
the slide is about basic concept of the clinical trials
From history and with case studies
An important body that overlooks the conduct of CT including safety issues
An Investigational New Drug Application (IND) is a request from a clinical study sponsor to obtain a...
research methodology in medicine
Development Safety Update Report
The Declaration of Helsinki is a set of ethical principles and guidelines for medical research invol...
An IND is a submission to the food and drug administration (FDA) requesting permission to initiate a...
The interview question series on clinical research is important for several reasons: Assessment of ...
Nill
For every B.PHARM, UG students
IRB REVIEW
Investigational New Drug application
![Investigational New drug application [INDA]](https://slidepub.com/thumb/5643/63215643.jpg)
