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Date of Publication: July 01, 2000
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Research Articles
Informed consent in clinical trials
Abstract:
The development of a new drug is a lengthy process. Once a promising compound is identified, it must be investigated in laboratory studies and tested on laboratory animals. After years of work, the newly developed drug is ready for clinical trials, or the testing on human volunteers.
Copyright and license ©Indian Journal of Medical Ethics 2016: Open Access and Distributed under the Creative Commons license ( CC BY-NC-ND 4.0), which permits only non-commercial and non-modified sharing in any medium, provided the original author(s) and source are credited.
