Geeta Ogra Bedi is a professional with a career spanning over 26 years in the Pharma and Biotech industry. She has expertise in auditing of Good Laboratory Practice (GLP), Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP) and CFR part 11 compliance. She has worked with small and large multinational companies and audited many pharmaceutical companies and Contract Research Organizations/Vendors globally covering pre- and post-marketing quality assurance programs in different therapeutic areas especially IND directed studies. She has managed and facilitated due diligence/ out-licensing of NCEs/ NCE co-development programs and has experience in handling MHRA/FDA/DCGI, etc. inspections and readiness for inspections in GxP area. Presently, she is on board with many global auditing companies for managing Quality Assurance programs.

Geeta holds a Master’s degree in Pharmacology from Hamdard college of Pharmacy, New Delhi, India.

Geeta holds a Master’s degree in Pharmacology from Hamdard college of Pharmacy, New Delhi, India.