Technical Resource by on

MDR & Usability regulations and standards

Topics covered:

    • Europe’s recent advancements in device and packaging regulations
    • Aligning MDR regulations with ISO standards
    • Discovering a disconnect between regulations for medical devices and their packaging systems
    • Designing sterile packaging for successful end-use

Interested in learning more about this topic? Book a virtual lunch & learn session with the PAXXUS technical team!