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Food and Drug Administration (FDA) Joins Pharma IQ's Viral Safety 2011 Conference
Date:8/22/2011

LONDON, August 22, 2011 /PRNewswire/ --

Santosh Nanda, Microbiologist/ Primary Reviewer, CBER, FDA and Rebecca Sheets, Vaccine Scientific and Regulatory Specialist, NIH/NIAID have announced their official participation at the Viral Safety 2011 conference due to take place from the 17th October to 19th October 2011 in NH München Dornach, Munich, Germany.

This year's conference has expanded its focus from solely viral safety to encompass mycoplasma, TSE and bacteria. The event will have a strong focus on prevention and regulatory compliance as well as offering a nature of discussion based and interactive sessions.

Systematically Characterising Adventitious Agent Tests for Biologics

At the conference, Rebecca Sheets will be discussing the policy perspective on adapting new testing methodologies, she will assess the breadth and sensitivity of routine adventitious agent tests and will cover the harmonisation of test methods (both existing and emerging).

On the other hand, Santosh Nanda will be sharing a regulatory perspective on how to evaluate the Safety of New Flu Vaccine Development Methods, he will assess the risks of the cell-based development process and will also Investigate the challenges and benefits of utilising cell based vaccine development and developing regulatory guidance to govern the process.

The Viral Safety 2011 conference aims at creating effective strategies to mitigate risk and enable prompt remediation of viral, prion and mycoplasma contamination - it will provide an interactive forum for learning best practices, keeping abreast of new developments and forging lasting business relationships.

20 biotech and biopharma experts are getting together this October to share updates and insights on how to escape contamination and get your products to market safely, speedily and successfully.

To view the conference programme (including ful
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SOURCE Pharma IQ
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