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Nitisha Pyndiah

Contact Details

United States

Bio

Nitisha Pyndiah is a Consultant for HartmannWillner where she provides professional advice to clients including strategic support for the development of biological, biotechnological, and biosimilar products during preclinical development and throughout the product lifecycle.
Nitisha has over six years of experience in biomedical research, biotechnology, clinical studies and regulatory affairs. Her experience was gained in international reputed institutions and through projects for major pharmaceutical companies.
Her expertise includes new technologies, virology, molecular biology, microbiology, immunology, quality control, quality assurance, audits, Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). She also has experience in regulatory support and advice; Chemistry, Manufacturing and Controls (CMC) review; scientific and regulatory gap analyses of Investigational Drug Applications (INDs); preparation of Quality Overall Summaries (QOS); preparation of General Investigational plans; preparation and support for FDA meeting documents; review and submission of expedited safety adverse event reporting; Orphan Drug Designations; preclinical studies; clinical trials and pediatric regulations for the EMA and FDA. She has been involved in technical, strategic, and operational regulatory affairs and has interacted both with the EMA and the FDA.
Nitisha was awarded a Distinction for her MSc and obtained a Young Investigator Award from the Conference on Retroviruses and Opportunistic Infections (CROI) during her PhD. As a member of the Regulatory Affairs Professional Society (RAPS), she attends RAPS chapter meetings and has obtained a regulatory affairs certificate in Pharmaceuticals from the RAPS.
Nitisha is currently preparing for her Regulatory Affairs Certification (RAC).
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Job History

HartmannWillner
Consultant
April 2016 - present