Medical devices

We offer tailored professional development options for the entire medical device sector. We are happy to advise you before you choose a training course and, of course, remain available to support you afterwards as well. Our high quality standards are also reflected in our ISO certifications in accordance with ISO 9001:2015 and ISO 21001:2018.

Have you not found the right seminar? We would be pleased to design a tailored in-house seminar for you. Some of our seminars also fulfil the requirements for recognition under § 15 FAO. Please feel free to contact us for further information.

In our media library, you will find tips, trends, and insights on Pharma and Healthcare available for download.

Are you interested in seminars in Pharma and Healthcare? Feel free to take a look here.

Regulatory Affairs, Quality & Risikomanagement

Advance your expertise in EU certification and international regulatory strategies. Gain in-depth knowledge of MDR/IVDR, MDCG guidances, ISO 13485, ISO 14971 and other technical standards,…

Advance your expertise in EU certification and international regulatory strategies. Gain in-depth knowledge of MDR/IVDR, MDCG guidances,…

Legal, Marketing & Sales

Advance your expertise in legally compliant marketing, strategic sales and medical affairs for medical devices. Deepen your knowledge of advertising law, medical device regulations,…

Advance your expertise in legally compliant marketing, strategic sales and medical affairs for medical devices. Deepen your knowledge of…

Artificial Intelligence

Discover how artificial intelligence is transforming the medical device industry. Advance your expertise in AI-driven documentation, the regulation of AI systems as medical devices and the…

Discover how artificial intelligence is transforming the medical device industry. Advance your expertise in AI-driven documentation, the…

Vigilance & Post-market

Advance your expertise in vigilance, post-market surveillance (PMS) and complaint management for medical devices. Gain practical knowledge of regulatory reporting, signal detection and…

Advance your expertise in vigilance, post-market surveillance (PMS) and complaint management for medical devices. Gain practical…

Clinical Affairs

From research and development to clinical application: advance your expertise in clinical investigation (ISO 14155), clinical evaluation and post-market clinical follow-up (PMCF) for medical…

From research and development to clinical application: advance your expertise in clinical investigation (ISO 14155), clinical evaluation…

Contact

We are happy to provide you with personal and individual advice.

Our professional development portfolio is extensive. We would be pleased to discuss your requirements with you personally and help identify the most suitable options from our range of offerings. Let our professional development experts advise you and feel free to contact us today.

Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de