483
Pratik Doshi, M.D.FDA 483 - Pratik Doshi, M.D. - March 07, 2025
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Record Details
An FDA inspection of Pratik Doshi, M.D., a bioequivalence clinical testing facility in Vadodara, Gujarat, India, identified one observation. The firm failed to meet general requirements for informed consent. Specifically, consent forms for a clinical research project included a statement that the study was "not of an experimental nature," which did not minimize the possibility of coercion or undue influence.
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ID · eb8a9a18-cb03-497a-8f74-e22c611a80a5