Avoiding Pitfalls in MDD to MDR Transition

ABOUT THE WEBINAR

Join us for an in-depth webinar addressing the challenges of transitioning from the Medical Device Directive (MDD/AIMDD) to the Medical Device Regulation (MDR) focusing on biological safety. Obtain valuable insights into MDR requirements, avoid common pitfalls and streamline the preparation and submission of your MDR documentation.

Our expert speakers will provide general guidance on conformity assessment for biocompatibility, reprocessing, sterile packaging, and both standard and non-standard sterilization methods. You can gain a clear understanding of the key differences between the MDD and MDR in these areas, as well as the documentation expectations of Notified Bodies.

In the second half, join an engaging panel discussion featuring Notified Body representatives. This interactive session is your opportunity to deepen your knowledge and ask our panel any burning question you may have.

Register now to secure your spot!

WEBINAR TOPICS

• Biocompatibility

• Reprocessing

• Sterile packaging

• Sterilization

• Your questions and answers

TIMING

Date: 27 February 2025, Thursday

Duration: 90 minutes