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  1. Library
  2. Recording: Overview of Exci...

Recording: Overview of Excipient Laws and Regulations in Europe



Tuesday, November 16, 2021 - 9:00am to 11:00pm EST

This webinar was intended to provide a road map for how the regulatory process in Europe works relative to the use of excipients with a focus on requirements for:
1. Excipient manufacturers/suppliers
2. Drug manufacturer/excipient users
3. European regulatory bodies and competent authorities

Learning/Awareness Objectives
Attendees will be provided with:
> Understanding of responsible European regulatory agencies and standards for excipients
> Understanding of local law/regulations for registration and/or import of excipients
> Excipient monograph regulatory and testing requirements
> Excipient information necessary for supporting drug applications
> General overview of Certificate of Suitability (CEP) process and when/how used
> Regulatory considerations for Atypical Actives and colorants.
> Emerging hot topics and challenges impacting excipients

Who should attend?
> Excipient manufacturers, users, distributors
> Regulatory Affairs
> Compendial Affairs
> Quality Affairs

$20.00 - $159.00
General Registration
$159.00
IPEC-Americas Members
$79.00
Students / Faculty
$20.00
Government Employees
$60.00
IPEC Europe Members
$79.00
Items Included in the Purchase of this Course
Presentation Icon

Overview of Excipient Laws and Regulations in Europe

Presentation: Ms. Yasemin Koybasi , Dr. Johanna Eisele, 123 min 23 sec
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