Webinar: The Regulation of Biotechnology Products

Webinar: The Regulation of Biotechnology Products
This webinar will provide an introduction to biotechnology products for regulatory affairs professionals.


Date: Tuesday 22 January 2019
Time: 12.00 - 13.00 (GMT)



Learning objectives

To understand:
  • The biotechnology products and how are they regulated
  • The characteristics of products and production processes
  • How they differ from other healthcare products
  • What are biosimilars


 
 
 

Target audience

  • This webinar is for new entrants to the profession, with at least 6 months of regulatory experience
  • Those whose regulatory experience is outside the EU

 
Presenter 

Tejash Shah works as a regulatory project manager in the CMC Biopharmaceuticals department of global regulatory affairs at GSK in Ware. Tejash is a qualified Pharmacist and has a master's degree from the University of Hertfordshire, and moved into the world of Regulatory Affairs in 2015. 

Tejash has a wide range of experience in Drug Discovery & Development with emphasis being on Formulation Department of monoclonal antibodies and other novel target antibody formats; such as domain antibodies and antibody fragment-conjugates.  


CPD

This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
 

How do I apply?

Simply login or create an account and register below. 

Course fees:
Type Member  Non-member 
Standard    £75+VAT £95+VAT 
 
 

Terms and conditions

Please read the training terms and conditions before booking this webinar. By booking this webinar, you are agreeing to the terms and conditions.
When
22/01/2019
Where
At Your Desk
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