IPEC Europe Webinar
Quality Agreement Guide and Template(s) 2017
Thursday 23 November 2017, 15:00-16:00 CET.
IPEC Europe members: €50 excl. VAT
Non-members: €75 excl. VAT
Professionals who have recently become engaged in customer/user management and for experienced professionals, a refresher on the latest developments in this important area.
Webinar objective :
This webinar will offer best practices and guidance on the content of an excipient Quality Agreement. Excipient suppliers will be introduced to the process of preparing their own Quality Agreement Template according to company standards, as the template format is intended to be flexible.
Ms Astrid Stockrahm-Uhling, Global QA Specialist, DFE Pharma.
Astrid is a graduate in Chemical Engineering and initially worked for a Contract Research Organisation in execution of Phase I and II Clinical Trials. She then joined JANSSEN-CILAG in 1995, spending 6 years as Clinical Research Manager and another 5 years in Quality Assurance responsible for Clinical Drug Supplies. In 2007 she joined DFE Pharma and took up the position of QA Manager with overall responsibility for all QA and Regulatory activities worldwide. Since 2014 she is Internal Advisor for GMP compliance and the company's official representative in IPEC Europe activities.
Astrid also led the task force responsible for the revision of the 2009 Quality Agreement Guide, and is a member of the GMP Guide revision team.
Webinar registration fees are non-refundable. Substitutions are acceptable. Webinar participants who are not able to attend must notify the IPEC Europe Secretariat (email@example.com) in writing the name of the substitute participant as soon as possible and no later than 21 November EOB.
Please contact the IPEC Europe Secretariat: firstname.lastname@example.org / +32 2 2 13 74 40