TRAINING COURSE | Webcast series: Global regulatory requirements for Drug Device Combination Products (DDCs)

Overview for the EU, US, China, and MENA region

Overview for the EU, US, China, and MENA region
February 20, 2026

Do not miss this webcast by FORUM • Institut für Management GmbH where ASPHALION MedTech expert Fran Rodríguez Gómez, PhD is participating!

The webcast consists of four sessions, each dedicated to a different region: 30th of April – EU Regulatory Landscape, 7th of May – US Regulatory Landscape, 13th of May – China Regulatory Landscape, and 7th of May – MENA Regulatory Landscape.

Each session will delve into essential topics, including:

  • Types of combination products and their definitions
  • Legislative framework governing these products
  • Quality requirements and necessary documentation
  • Post-approval activities and their management
  • Submission process for regulatory approval

 

These sessions are ideal for professionals looking to speed up approval for DDCs in EU and non-EU countries.

For further information and registration: https://bit.ly/3OtdR3O

Need Help in your Regulatory requirements? Contact us: [email protected]

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