Preconference Workshops
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Thursday, May 11th
09:00 – 10:00 CESTMDCG 2022-14: Game-Changer or 'Shopping List' for MDR Implementation?Location: Pearl 2
Moderator: – TÜV SÜD Medical Health Services
Moderator: – Qserve Group
Presenter: – European Commission
Presenter: – TUV SUD Product Services
Presenter: – BSI
Presenter: – Federal Agency of Medicines and Health products
Medical DevicesDomain: Product Development & RegistrationKnowledge Area: Regulatory Guidance
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Thursday, May 11th
13:45 – 14:45 CESTMDR Art. 117 for Combination Products After 2 years. Still the same? State of Play from EMA, NB and IndustryLocation: Pearl 2
Moderator: – Benefits Regulatory Consulting
Presenter: – Ypsomed AG
Presenter: – anteris medical GmbH
Presenter: – EMA
Presenter: – BSI Group
PharmaceuticalsDomain: Product Development & RegistrationKnowledge Area: Regulatory Guidance
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Friday, May 12th
10:45 – 11:45 CESTMedical Device Software: Top Recurrent Regulatory Deficiencies from Both FDA and Notified BodiesLocation: Pearl 1
Moderator: – RQM+
Presenter: – RQM+
Presenter: – TÜV SÜD Product Services
Medical DevicesDomain: Product Development & RegistrationKnowledge Area: Regulatory Guidance
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Friday, May 12th
14:00 – 15:00 CESTStrategic approaches in pregnancy and paediatrics: Is it time for a paradigm shift?Location: Pearl 1
Moderator:
Moderator: – UCB
Presenter: – AstraZeneca
Presenter: – UCB Pharma
Presenter: – European Medicines Agency
PharmaceuticalsDomain: Product Development & RegistrationKnowledge Area: Regulatory Guidance
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Friday, May 12th
15:30 – 16:30 CESTEuropean Expedited Approval Pathways in a Global ContextLocation: Carmine & Charcoal
Moderator: – Parexel
Presenter: – CSL Behring AG
Presenter: – European Medicines Agency
PharmaceuticalsDomain: Product Development & RegistrationKnowledge Area: Regulatory Guidance