SFL and its highly-experienced, cross-functional team offer accredited training courses where participants will gain insight into both the basics as well as the latest developments in Regulatory Affairs, Quality Assurance, Reimbursement, Supply Chain and Medical Communications for Drugs, Devices, In vitro Diagnostics, and Combination products.
The first training, entitled ‘Introduction to EU Pharmaceuticals Regulatory Affairs, will be held on 10 November, 2 to 5 pm CET, and will cover key aspects of Regulatory Affairs in the EU with a focus on medicinal products:
The European Legislative Framework
Pre-submission activities with the European Medicines Agency
Clinical Trial Application Dossier
Marketing Authorization Application Procedures in Europe
Members of Medtech & Pharma Platform (MPP), Rare Disease Action Forum (RDAF), Swiss Association of Pharmaceutical Professionals (SwAPP), Swiss Biotech Association (SBA) and Swiss Medtech will benefit from fee reduction.
SFL also offers customized trainings, at your company’s site or online, and tailored to your company’s needs as part of its . For more information, please contact us at firstname.lastname@example.org.