Overview and current procedural status
Webcode 26122661
Dr. Alexander Meier
Morgan, Lewis & Bockius LLP, Munich, GERMANY
Life Sciences Regulatory Partner;
Alexander Meier is a German trained lawyer with more than 25 years of relevant professional experience, specialised in European and German pharmaceutical law concerning research, development, authorisation and commercialisation of medicinal products and medical devices.
He started his professional career in 2000 in Munich (DE) and worked both as outside counsel for various law firms as well as for over 13 years as an in-house lawyer, including for Novartis and Moderna. In February 2026 Alexander Meier joined the law firm Morgan, Lewis & Bockius as Partner in their Munich office.
Alexander Meier is the author of numerous publications, a regular speaker at international conferences, and lecturer at the CEIPI of the University of Strasbourg (FR).
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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 current EU pharmaceutical legislative framework. In approximately 90 minutes, you will understand the status of the legislative process, the scope of the new Regulation and Directive, and how related legal acts such as the Variation Regulation and the Critical Medicines Act are affected.
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 current EU pharmaceutical legislative framework. In approximately 90 minutes, you will gain clarity on the status of the legislative process, the scope of the new Regulation and Directive, and their impact on related legal acts such as the Variation Regulation and the Critical Medicines Act. The module also covers the current legal status and regulatory requirements of ePI. By the end, you will be able to place the key legislative changes in context and assess their relevance for your day-to-day regulatory work.
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.
Dr. Alexander Meier
The legal framework part 1 - overview and current procedural status 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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