EU Excipient Risk Management Guide

About this course

Time: 10am EST - Duration: 1 hr

This webinar will review the EU draft guidance on Excipient Risk Assessment published 7 February 2026 and latest news regarding its implementation.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

Course outline

• 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

Venue

Webinar

Please register through the ‘book now’ button on the right to receive joining instructions

Tutors

We believe that our team of experts are the best available. Not only have they got years of experience in the industry, but they are committed to tutoring and helping those inside the industry to improve and raise the standards. We understand that you attend courses to learn about the latest regulations and to get your questions answered.

Our expert for this webinar is:

Chris Moreton

• 

  Mrs Janeen Skutnik
  Vice President
  BSc

  • [email protected]
  • + 1 857 277 0060

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