Webinar on Matured / Established Products Regulatory Support & Models



Join us for LIVE WEBINAR on 12 Jan @ 11am EST
Matured/
Established
Products
Regulatory
Support &
Models
Speaker
Chand Sishta

Director, Global Regulatory Sciences
Matured Products

Bristol-Myers Squibb


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Matured products go through multiple decisions in Global organization like: Keep or divest? Same teams or different teams to handle them? For regional support, who should pay? and more. All these stemming from cost pressures in global markets and changing regulatory environment. Whether you are part of the Regulatory group in an emerging/mid-size/large global Biopharma organization with aging product portfolio or a Generic company with multiple products whose licenses need to be maintained, do not miss this upcoming Webinar on Matured Products.

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:

Tick Bullet   What is a matured/established product

Tick Bullet   How do health authorities view matured/established products

Tick Bullet   What challenges are encountered for these products in international markets

Tick Bullet   How does information gathered via regulatory intelligence impact these products

Tick Bullet   How do these Matured Products thrive when generics are available in marketplace

Tick Bullet   How to manage compliance effectively

About Our Speaker:

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.