Daniel Gordin's Location
New York, New York, United States
Daniel Gordin's Work
- Executive Director @ Sunovion Pharmaceuticals
- Senior Director @ Glenmark Pharmaceuticals
- Regulatory Affairs Consultant @ Regulatory Affairs Consultant
- Executive Director, Drug Regulatory Affairs @ Novartis
- Associate Director, Regulatory Affairs @ Forest Laboratories (now Allergan)
- Director, Regulatory Affairs @ Synthelabo Research
- Associate Director, Regulatory Affairs @ Otsuka Pharmaceutical Companies (U.S.)
- Head, Regulatory Affairs @ Leiras Pharmaceuticals
- Pharmacokinectic Reviewer @ FDA
Daniel Gordin's Education
- Medical University of South Carolina
Ph.D. (Pharmaceutical Science)
1983 - 1989 - Medical University of South Carolina
B.S. (Laboratory Science)
1981 - 1983 - University of South Carolina
B.S. (Biology)
1976 - 1980
Daniel Gordin's Skills
- Regulatory Affairs
- FDA
- Pharmaceutical Industry
- Pharmacokinetics
- Strategy
- Product Development
- Regulations
- Regulatory Submissions
- Clinical Development
- Clinical Trials
Daniel Gordin's Summary
Daniel Gordin, based in New York, New York, United States, is currently a Executive Director at Sunovion Pharmaceuticals Inc., bringing experience from previous roles at Glenmark Pharmaceuticals, Regulatory Affairs Consultant, Novartis and Forest Laboratories (Now Allergan). Daniel Gordin holds a 1983 - 1989 Ph.D. in Pharmaceutical Science @ Medical University of South Carolina. With a robust skill set that includes Regulatory Affairs, FDA, Pharmaceutical Industry, Pharmacokinetics, Strategy and more, Daniel Gordin contributes valuable insights to the industry. Daniel Gordin has 3 emails on RocketReach.
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