Samrat Sisodia Email & Phone Number
Vice President Regulatory Affairs | Quality Assurance | Pharmacovigilance @ Harrow
5 free lookup(s). No credit card required.
If you need more lookups,
subscriptions start at $34 USD/month.
Samrat Sisodia Location
- Farmington, CT, US
Samrat Sisodia Work
- Vice President Regulatory Affairs | Quality Assurance | Pharmacovigilance @ (April 2024 - Present)
- Vice President Regulatory Affairs and Quality Assurance @ (August 2020 - April 2024)
- Vice President Regulatory Affairs - North America @ (April 2019 - July 2020)
- Vice President of Scientific Affairs (RA and Compliance) @ (October 2018 - April 2019)
- AVP Scientific Affairs (RA and Compliance) @ (January 2018 - September 2018)
- Senior Director Regulatory Affairs and Compliance @ (March 2015 - January 2018)
- Head Regulatory Affairs @ (October 2011 - March 2015)
- Regulatory Affairs Manager @ (October 2007 - October 2011)
- Regulatory Affairs Asso to Manager @ Pharmaceuticals (October 2003 - October 2007)
Samrat Sisodia Education
- Monarch University - Switzerland
Doctor of Philosophy (D.Phil / Ph.D.) (Regulatory Science)
2012-2016 - Harvard University
Certification Course in Fundamentals of Clinical Trials
2014-2014 - Northwestern University - Kellogg School of Management
Executive Development Program (Regulatory Affairs)
2014-2014 - Massachusetts Institute of Technology
Certification Course in Solid State Chemistry
2013-2013 - University of California, Berkeley
Certification Course in Descriptive Statistics
2013-2013 - Columbia Southern University
Master of Business Administration (MBA) (Marketing Management)
2010-2012 - Devi Ahilya Vishwavidyalaya
Masters (Pharmaceutical Chemistry)
2001-2003 - Devi Ahilya Vishwavidyalaya
Bachelors (Pharmaceutical Chemistry)
1998-2001
Samrat Sisodia Skills
- Regulatory Affairs
- NDA
- ANDA
- IND
- Generics
- CMC submission strategies
- Regulatory Strategy
- Research Project Management
- FDA negotiations
- Regulatory Requirements
- Regulatory Submissions
- Regulatory Filings
- Chemistry
- eCTD
- Regulatory Risk
- Pharmaceutical Development
- Drug Development
- FDA
- Generic Programming
- Sop
- Formulation
- Pharmaceutical Industry
- CMC
- GMP
- CRO
- CMC Regulatory Affairs
- CTD
- GLP
- Change Control
- Technology Transfer
- Pharmaceutics
- CAPA
- Pharmacovigilance
- R&D
- Validation
- Strategy
- Abbreviated New Drug Application (ANDA)
- CRO Management
- Common Technical Document (CTD)
- Good Laboratory Practice (GLP)
- Research and Development (R&D)
- New Drug Application (NDA)
- U.S. Food and Drug Administration (FDA)
- Standard Operating Procedure (SOP)
- FDA Audit
- Quality Assurance
- Research and Development R&d
- Project Management
- Regulatory
- Good Laboratory Practice Glp
- Standard Operating Procedure Sop
- New Drug Application Nda
- Abbreviated New Drug Application Anda
- Cell Culture
- Common Technical Document Ctd
- u.s. Food and Drug Administration Fda
- Strategic Planning
- Marketing
- u.s. Food and Drug Administration
- Abbreviated New Drug Application
- Standard Operating Procedure
- New Drug Application
- Common Technical Document
- Good Laboratory Practice
- Research and Development
Samrat Sisodia Summary
- Samrat Sisodia, based in Farmington, CT, US, is currently a Vice President Regulatory Affairs | Quality Assurance | Pharmacovigilance at Harrow. Samrat Sisodia brings experience from previous roles at Palatin Technologies, Glenmark Pharmaceuticals and Breckenridge Pharmaceutical, Inc.. Samrat Sisodia holds a 2012 - 2016 Doctor of Philosophy (D.Phil / Ph.D.) in Regulatory Science @ Monarch University - Switzerland. With a robust skill set that includes Regulatory Affairs, NDA, ANDA, IND, Generics and more. Samrat Sisodia has 2 emails and 2 mobile phone numbers on RocketReach.
Looking for a different Samrat Sisodia?
Find contact details for 700 million professionals.
Others Named Samrat Sisodia
Top Harrow Employees
G2 Crowd Trusted
300K+ Plugin Users
© 2026 RocketReach.co