Webcode 26122663
Anna Wehage
Pharma Deutschland e.V., Berlin, GERMANY
Anna Wehage is currently working as a Senior Advisor for National and European Health Policy at Pharma Deutschland e.V. With over seven years of experience in the pharmaceutical industry and another seven years in association work, she combines hands-on expertise in pharmaceutical manufacturing and quality processes with a strong background in health policy and regulatory affairs at both national and European levels.
Previously, she served as Head of Quality Department in the pharmaceutical industry, where she gained extensive experience in regulatory processes within pharmaceutical manufacturing and quality control. Anna Wehage holds a Master's degree in Drug Regulatory Affairs from the University of Bonn and a Diploma in Biology from the Technical University of Kaiserslautern.
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Event - 390€ plus tax
The fee for a single access valid for 90 days is 390 € (plus VAT). During this period, you can access the content as many times as you like. You will also receive the presentation materials for download.
Event - 390€ plus tax
The fee for a single access valid for 90 days is 390 € (plus VAT). During this period, you can access the content as many times as you like. You will also receive the presentation materials for download.
Jean-Marie Bayhurst
Konferenzmanager Pharma & Healthcare
+49 6221 500-685
j.bayhurst@forum-institut.de
This recording delivers a clear overview of the new supply shortage obligations under the EU pharma reform. In approximately 90 minutes, you will understand the new prevention and risk planning requirements, the coordination between EMA and national competent authorities, and the practical implications for manufacturers and marketing authorisation holders.
This recording of a live webcast series provides a structured, practice-oriented update on the EU pharmaceutical reform. The webcast consists of four individual modules, each approximately 90 minutes long, which are available separately or as a complete bundle at a reduced price. This course covers one module. The bundle "Update EU Pharma Legislation - The Full Series" can be found via the webcode 60012660.
The recording of this module provides a structured overview of the new supply shortage obligations under the EU pharmaceutical reform. In approximately 90 minutes, you will gain clarity on the new requirements for shortage prevention and risk planning, the coordination mechanisms between EMA, national competent authorities and pharmaceutical companies, and the reporting and monitoring obligations introduced by the reform. The module also addresses the practical implications for manufacturers, marketing authorisation holders and supply chain management, as well as the interplay with the Critical Medicines Act. By the end, you will be able to assess the operational impact of the new shortage framework on your organisation and identify the measures needed to ensure compliance.
The recorded content is available to you flexibly - ideal for reviewing the topics at your own pace or looking up specific sections as needed. Access to the recording is available for 90 days after purchase.
Anna Wehage
Supply shortages and supply security This course is a recorded module from a live webcast series held in June 2026. You will gain access to all content flexibly - ideal to go through the topics at your own pace or revisit specific sections as needed. Access to the recording is available for 90 days after purchase. The content reflects the status at the time of the event.
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