Webcode 26122664
Dr. Angela Vogt-Eisele
CENCORA PharmaLex, Mannheim, GERMANY
Dr. Angela Vogt-Eisele has over 15 years of experience in the pharmaceutical industry supporting nonclinical and clinical development programs for small molecule drugs, advanced therapy medicinal products, biologics, food supplements and medical devices. One of her central areas of expertise lies in the field of environmental risk assessments (Europe, USA and world-wide). Prior to joining Cencora PharmaLex, Angela worked at Sygnis Bioscience GmbH as head of the in vitro department (2007-2012) being responsible for research and development in the area of stroke and dementia. Dr. Angela Vogt-Eisele holds a Diploma in Biology (University of Tübingen, focus: Molecular Genetics, Biochemistry, Immunology) and a doctoral degree (Dr. rer.nat, Max-Planck-Institute for Polymer Research and University of Mainz).
online
online
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 evolving ERA requirements under the EU pharmaceutical reform. In approximately 90 minutes, you will understand the current legal framework, the changes proposed in the new directive, how ERAs integrate into lifecycle management, and how to handle legacy compounds and other special cases.
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 evolving Environmental Risk Assessment requirements under the EU pharmaceutical reform. In approximately 90 minutes, you will gain clarity on the current legal framework, the rationale behind the tightening of existing requirements, and the key changes and remaining unknowns in the proposed directive. The module also addresses the integration of ERAs into lifecycle management, the handling of legacy compounds authorised before 2006, and special cases such as endocrine and persistent active substances. By the end, you will be able to assess the ERA-related obligations relevant to your portfolio and identify the steps needed to ensure compliance under the new framework.
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. Angela Vogt-Eisele
Environmental risk assessment (ERA) 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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