In Consulting Services

PharmaNet offers a comprehensive range of early- and late-phase consulting services on topics including: international regulatory affairs; scientific and medical affairs; quality; risk management; chemistry, manufacturing and controls; as well as biopharmaceutical investor issues.

Biography

Gregory M. Hockel, MBA, PhD

Senior Vice President, Regulatory Affairs Worldwide
504 Carnegie Center
Princeton, NJ 08540
USA

Tel: 609 951 6862
Fax: 609 720 5564

E-mail: ghockel@pharmanet.com

Expertise: Worldwide regulatory strategy, submissions, safety, compliance, and supply management

 

Dr. Hockel has more than 27 years of experience pharmaceutical, biotechnology, and CRO industry experience, including more than 22 years in regulatory affairs. On the pharmaceutical side of the industry, Dr. Hockel has held senior-level regulatory positions at Pfizer Central Research, British Biotech, and Guilford Pharmaceuticals. Throughout his career, he has been extensively involved in planning, compiling, and submitting numerous NDAs/BLAs and INDs. Dr. Hockel has also led initiatives involving drug safety, GCP auditing, compliance, and clinical-trial supply management.

 

PharmaNet Development Group, Inc.504 Carnegie Center, Princeton, NJ 08540Tel 609 951 6800Fax 609 514 0390