EU Excipient Risk Management Guide

Thursday, June 19 2014
10:00 am – 11:00 am

This event was posted by NSF Health Sciences

Location: Webinar

This webinar will review the EU draft guidance on Excipient Risk Assessment published 7 February 2013 and latest news regarding its implementation. We will review how the European Union proposes to assess and rank risk and establish risk profiles for excipient manufacturers, what GMPs are applicable for excipients and what companies are doing to enhance their vendor management programs.

What You Will Learn

  • Review the EU Guidance on Excipient Risk Assessments (draft)
  • How to establish a risk profile for an excipient manufacturer
  • Status of applicable GMPs for excipients, which countries are taking the lead in this area, and what you need to know to be compliant

Share MassBio

 

BioProcess

Janitronics

EvaluatePharma


 

MassBio