Explore recent issues of Contract Pharma covering key industry trends.
Read the full digital version of our magazine online.
Behind every facility expansion, technology investment, and quality milestone in the CDMO sector is a leadership team making deliberate choices about where to focus, how to grow, and when to take calculated risks.
Stay informed! Subscribe to Contract Pharma for industry news and analysis.
Get the latest updates and breaking news from the pharmaceutical and biopharmaceutical industry.
Discover the newest partnerships and collaborations within the pharma sector.
Keep track of key executive moves and promotions in the pharma and biopharma industry.
Updates on the latest clinical trials and regulatory filings.
Stay informed with the latest financial reports and updates in the pharma industry.
A video roundup of the week’s top industry news stories.
Expert Q&A sessions addressing crucial topics in the pharmaceutical and biopharmaceutical world.
In-depth articles and features covering critical industry developments.
Access exclusive industry insights, interviews, and in-depth analysis.
Insights and analysis from industry experts on current pharma issues.
A one-on-one video interview between our editorial teams and industry leaders.
Listen to expert discussions and interviews in pharma and biopharma.
Contract Pharma Stream offers a centralized destination where users can watch expert-led sessions anytime, anywhere
A detailed look at the leading US players in the global pharmaceutical and BioPharmaceutical industry.
Browse companies involved in pharmaceutical manufacturing and services.
Comprehensive company profiles featuring overviews, key statistics, services, and contact details.
A comprehensive glossary of terms used in the pharmaceutical and biopharmaceutical industry.
Watch in-depth videos featuring industry insights and developments.
Download in-depth eBooks covering various aspects of the pharma industry.
Access detailed whitepapers offering analysis on industry topics.
View and download brochures from companies in the pharmaceutical sector.
Explore content sponsored by industry leaders, providing valuable insights.
Stay updated with the latest press releases from pharma and biopharma companies.
Explore top companies showcasing innovative pharma solutions.
Meet the leaders driving innovation and collaboration.
Engage with sessions and panels on pharma’s key trends.
Hear from experts shaping the pharmaceutical industry.
Join online webinars discussing critical industry topics and trends.
A comprehensive calendar of key industry events around the globe.
Live coverage and updates from major pharma and biopharma shows.
Find advertising opportunities to reach your target audience with Contract Pharma.
Review the editorial standards and guidelines for content published on our site.
Understand how Contract Pharma handles your personal data.
View the terms and conditions for using the Contract Pharma website.
What are you searching for?
Seth V. Hetherington, M.D., senior vice president of Clinical and Regulatory Affairs at Icagen, Inc., will be leaving the company at the end of the year.
December 21, 2010
By: Tim Wright
Seth V. Hetherington, M.D., senior vice president of Clinical and Regulatory Affairs at Icagen, Inc., will be leaving the company at the end of the year. Greg C. Rigdon, Ph.D., vice president, New Product Development, will assume Dr. Hetherington’s role, taking on responsibility for the company’s clinical development efforts. P. Kay Wagoner, chief executive officer of Icagen, said, “Dr. Hetherington has provided outstanding leadership to Icagen’s clinical development efforts over the past four years. While we are of course disappointed, we understand his decision to return to his background in the area of infectious diseases. We thank him for his outstanding service to Icagen and wish him all the best in his future endeavors.” Dr. Wagoner continued, “Our progress in completing our submission to the FDA in support of the clinical development of ICA-105665 remains on track. Dr. Rigdon, who will assume leadership of the clinical effort, has been deeply involved in our epilepsy and pain program since its inception. We are confident that there will be no loss of continuity in our epilepsy and pain program as a result of these management changes.” Prior to joining the company, Dr. Rigdon spent ten years in clinical development and central nervous system pharmacology at Glaxo Wellcome, where he led the team responsible for the successful filing of a sNDA for Lamictal, an approved anti-epileptic.
Get the latest Contract Pharma news, insights and analysis in your Google Search and AI experiences.
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !