Events & webinars

Expand your knowledge with our expert-led events around the topics of testing and regulatory compliance. Join our upcoming live webinars to connect with our experts and bring your own questions to the discussion or explore our library of past recordings to learn at your own pace.
Measurlabs events
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Webinar: PPWR in practice: requirements and laboratory testing

Wednesday, March 25, at 2-3 PM (EET)

Join our Testing Expert, Niko Markkinen, to gain clarity on what the PPWR (Packaging and Packaging Waste Regulation) means in practice. You will get an overview of the regulation and its practical implications, and learn more thoroughly about what type of testing your products need to meet the regulatory criteria.

During the webinar, you will learn at least the following:

  • What requirements does the new PPWR present?

  • What is the timeline of the changes?

  • What you need to test and how: heavy metals, PFAS, recyclability, etc.

As always, there will be time for audience questions after the presentation.

Webinar: Streamlining EU MDR approval: Re-using your FDA preclinical and clinical data

Thursday, March 26, at 6 pm (EET) / 12 pm (ET) / 9 am (PT)

In this webinar hosted together with Mantra Systems, we will walk you through how to reuse and adapt preclinical testing, clinical data, and regulatory documentation from your FDA submission to ensure the most efficient possible route to CE-marking and EU MDR compliance. During the one-hour session, we will cover the following:

  • Which components of the Technical File can be repurposed and which are unique to the EU MDR

  • Key differences between FDA and EU MDR testing requirements

  • How risk assessment drives testing decisions, including the use of Biological Safety Assessment (BSA) and Biological Evaluation Plan (BEP) to justify testing scope and minimize unnecessary studies

  • Whether clinical data from the US can be used to support conformity in the EU

There will also be time for audience questions after the presentation.