Accelerating Vaccine Development: Regulatory, Biosafety, and Clinical Strategies

This webcast will begin on Sept. 9, 2014, 11 am EDT and Tuesday, Sept. 16, 2014, 15:00 CET


Health authorities and vaccine manufacturers worldwide are seeking efficacious, more cost-effective vaccines while expediting vaccines development to serve larger populations and meet potential pandemic threats. Additionally, vaccine developers must navigate a variety of regulatory, biosafety, and clinical development challenges to meet these demands.

This webcast will address vital strategies for the development of seasonal and pandemic influenza vaccines, as well as universal vaccines. A regulatory expert will provide a perspective on new and evolving vaccine approval trends and challenges among health authorities worldwide.

Key Learning Objectives:

• Understand regulatory challenges in developing vaccines in a global marketplace
• Review biosafety test methods for various vaccine platforms
• Learn how viral challenge testing can demonstrate efficacy earlier in the development process

Archie Lovatt, PhD
Scientific Operations Director
SGS Vitrology

Robert Lins, MD, PhD
Senior Clinical Advisor – Clinical Research
SGS Life Science Services

Rajesh K. Gupta, Ph.D.
Principal Consultant
Biologics Quality & Regulatory Consultants, LLC

Rita Peters

Editorial Director
BioPharm International

This is a FREE streaming audio Webcast and does not require a phone line. If you have any questions regarding this Webcast, please contact Sara Barschdorf,

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