With the deadline for implementing the new Medical Device Regulation (MDR) fast approaching, it is crucial for medical device manufacturers to understand the updates that have driven changes in the ISO 11607 packaging standards. This webinar will provide an in-depth look at the latest updates to the MDR and their significant impact on packaging requirements.
Participants will gain insights into how these regulatory changes have prompted revisions in the ISO 11607 standard, which outlines the requirements for packaging materials, sterile barrier systems, and validation processes. The session will explain the specific updates to the MDR that have necessitated these changes and what they mean for manufacturers who must comply with these new standards.
Attendees will learn about the practical implications of these changes, including how to adapt their current packaging processes to meet the updated requirements. The webinar will highlight key aspects such as the importance of ensuring that packaging systems maintain sterility, integrity, and safety throughout their lifecycle.
By the end of this webinar, viewers will have a clear understanding of the new MDR-driven changes to ISO 11607 and the steps they need to take to achieve compliance before the implementation deadline. This session is essential for packaging engineers, quality assurance professionals, and regulatory affairs specialists involved in medical device manufacturing, providing them with the knowledge and tools needed to navigate the new regulatory landscape and ensure their packaging processes meet the highest standards.