Webinar on Matured / Established Products Regulatory Support & Models
Join us for LIVE WEBINAR on 12 Jan @ 11am EST
Our speaker, Chand Sishta, Director Global Regulatory Sciences, Matured Products at Bristol-Myers Squibb will focus on current challenges and what the future holds for them. Some of the points being covered are listed below:
How do health authorities view matured/established products
What challenges are encountered for these products in international markets
How does information gathered via regulatory intelligence impact these products
How do these Matured Products thrive when generics are available in marketplace
How to manage compliance effectively
Chand Sishta is currently Director, Global Regulatory Sciences, Matured Products at Bristol-Myers Squibb Company located in Lawrenceville, NJ.
Chand received his Ph.D. from the University of British Columbia, Vancouver, B.C. in 1990 and completed a Post-Doctoral Fellowship at Northwestern University from 1990 to 1992. He started as a discovery scientist with Union carbide Corporation in Bound Brook, NI in 1992 and this role led to significant interactions with large manufacturing plants. Consequently, he worked as a FDA Regulatory Manager at Union Carbide. Chand then worked for Bristol-Myers Squibb from 2000 to 2005 as Quality Assurance for the development division of BMS located in New Brunswick, NJ. From 2005 to 2011, Chand worked for Pfizer as Regulatory CMC located in Peapack, NJ.