Sayed Ahmed
- Role
- Associate Director, Global Regulatory Affairs at Merck
- Location
- Princeton Junction, NJ, US
- LinkedIn followers
- 500 followers
Experience
Associate Director, Global Regulatory Affairs
Nov 2015 — Present
Provide regulatory guidance to discovery and full development teams for the registration of new veterinary pharmaceuticals in the US. Coordinate regulatory input to exploratory and full development plans that include US & Global strategies. Influence development plans to assure execution of studies to support quality and timely product approvals. Prepare and file applications, interface with FDA to effect high quality communications to achieve registrations.
Skills
- Gcp
- Cmc Regulatory Affairs
- Quality Auditing
- European Medicines Agency
- Sop
- Regulatory Affairs Certification
- Clinical Trials
- Veterinary Drugs Directorate - Canada
- Quality Assurance
- Cvm
- Clinical Development
- Drug Development
- Technology Transfer
- Regulatory Submissions
- Vaccines
- Apvma - Australia
- Gmp
- Pharmaceutical Industry
- Change Control
- Regulatory Affairs
- Chemistry
- Lifesciences
- R&D
- Toxicology
- V&V
- Fda
- Biotechnology
- Glp
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