Bio-IT World Podcast: Technology Challenges and Outlook for Drug Safety Management in Clinical Trials
This podcast will discuss the drug safety regulation challenges that the biopharmaceutical industry is facing in clinical trials and the emerging new technologies that can help researchers to address them. “Dr. Barton Cobert, President, BLCMD Associates and Fran Nolan, VP, Quality Assurance, Medidata address the following questions:
- What are the challenges associated with drug safety in clinical trials?
- How can a clinical study sponsor be better prepared for regulatory agency safety inspections?
- What is the outlook of technology in safety data management?
Dr. Barton Cobert
President
BLCMD Associates
bcobert@gmail.com
Fran Nolan
Vice President, Quality Assurance
Medidata Solutions Worldwide
fnolan@mdsol.com
Please register to listen to the podcast