Month: November 2024

With the IVDR entering into force on 26 May 2022 in Europe, manufacturers have switched from Europe to the US market as their primary entrance market. To assist the manufacturers, Gsap has joined forces with MDC Associates, a leading US company in the field of IVD, to bring the most updated information to ease navigation through the changing regulatory path.

Join this insightful webinar, led by Gsap and MDC experts, to hear about the latest IVD regulatory updates in the US and their implications for Israeli manufacturers.

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Process validation in the medical device industry plays a crucial role in ensuring a successful and effective manufacturing flow. The various challenges associated with process validation can be demanding and often require innovative, out-of-the-box solutions.

Gsap, in collaboration with Flex, has joined forces to address the most common challenges in the process validation (PV) process. To contribute to the successful completion of PV, we hope to impart to our community our vast professional knowledge and practical expertise.

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This webinar offers comprehensive insights into the medical device lifecycle, from the initial spark of an idea to the successful market launch.

Gain expert guidance on transforming your concept into a market-ready product, focusing on streamlining the transition from R&D to manufacturing, ensuring product quality and operational efficiency, and leveraging innovative packaging solutions, prioritizing safety, sustainability, and user satisfaction. Whether navigating development challenges, optimizing production processes, or aiming to achieve long-term success in the competitive medical device market, this webinar equips you with practical strategies and tools to stay ahead in the industry.

🎥 Watch the full recording below: