WEBCAST SERIES | Global regulatory requirements for DDC products

Announcing Our Participation in the Global Webcast Series on Regulatory Requirements for Drug-Device Combination Products from FORUM INSTITUT, GmbH!

Announcing Our Participation in the Global Webcast Series on Regulatory Requirements for Drug-Device Combination Products from FORUM INSTITUT, GmbH!
October 28, 2024

We’re pleased to share that Asphalion’s expert, Fran Rodríguez Gómez, will be featured in the upcoming webcast series on Global Regulatory Requirements for Drug-Device Combination Products (DDCs), hosted by the Forum Institut. This series offers a comprehensive exploration of the latest regulatory standards, insights, and best practices for DDCs, designed to support professionals in navigating the evolving landscape of healthcare regulations.

This webcast series provides an invaluable opportunity for professionals involved in regulatory affairs, clinical affairs, quality assurance, and product development to stay updated on current trends and requirements. Fran brings extensive experience and insights in regulatory pathways, compliance, and strategic planning for DDCs and will share key takeaways to support companies in aligning with global regulatory frameworks.

Key Benefits of Attending:

  • Meet four (local) experts that will share in-depth knowledge with you!
  • Obtain practical RA/CMC know-how for emerging markets!
  • Integrate the webcast sessions conveniently into your daily work routine!
  • Missed a live session? No problem! Make profit from the recording that is available after each individual webcast!

Have a look at the full programme here: WEBCAST SERIES: Global Regulatory requirements for DDC Products 

As a special offer, we are pleased to extend a 10% discount on each registration when accessed through the link: Discounted Registration

We invite you to join us for this important webcast series, where you’ll benefit from expert insights, practical advice, and the opportunity to connect with other professionals in the field, as well as gaining a better understanding of the additional and differing regulatory requirements and procedures in the different regions.

For further information: [email protected]

 

 

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