Digital MedTech Roundtable 2026.

The EU Packaging Regulation (PPWR), which came into force on 11 February 2025, and the PFAS limits that will apply from August 2026 pose considerable regulatory challenges for medical technology manufacturers. Unclear responsibilities between Development, Regulatory Affairs, Purchasing and Packaging Engineering as well as a lack of transparency in the supply chain harbour the risk of hidden non-compliance, which can lead to delays in product approvals, post-authorisation procedures or significant budget burdens due to redesigns.
Prepare your company specifically for this by identifying critical substances and suppliers and implementing proven best practices from the value chain.

As part of the Digital MedTech Roundtable, we will explain specific pitfalls that jeopardise packaging and product strategies - such as exceeding PFAS limits in blister packs or films that could compromise sterile barriers or recyclability. You will gain practical insights into how agile methods such as Design for Six Sigma, the Lean Progress Model and early risk analyses can systematically minimise these risks.
The roundtable offers interactive sessions, breakout rooms and networking opportunities to avoid supply interruptions, regulatory sanctions or market launch delays in the long term.