Sudipta Chakraborty

1st January, 1970

Sudipta Chakraborty

I have experience writing regulatory documents, including clinical study reports, protocols, and investigator’s brochures, in a variety of therapeutic areas. I also lead and am committed to the development process of patient-forward summaries that communicate clinical trial results in a non-promotional, unbiased, and easy-to-understand manner for both the patient community and the general public.


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