Medical Device Package Testing: Is Shelf-Life Testing Necessary?
About the webinar
Many times companies are keenly focused on developing the product that goes inside the box and miss critical requirements for the package that is intended to protect it. Designing safe packaging system that will protect the products during shelf life, while simultaneously complying with FDA or international health and safety regulations is essential. As well as developing an appropriate test plan for package performance testing is of utmost importance with the globalization of the medical device industry.
Topics
During this webinar, we will share insights and test plan to demonstrate how focusing on the packaging system for your product can help to save you time and avoid delays in your product development, including:
- Overview of various testing standards required to get your product to market
- The current status and expectations of the FDA
- How to design a test plan to meet the shelf-life requirements
Who should attend?
Managers, directors, engineers, and scientists responsible for research and development, product development, quality assurance, and regulatory compliance. Further, procurement, business leaders, and project management personnel responsible for requesting testing quotations.
When?
June 12th 2023
15:00 - 16:00 (CET)
Where?
Speaker
Dr. Sunny J. Modi is a Director of Package Testing for Eurofins Medical Device Testing with 10 years of experience focusing on creating and testing packaging materials. He specializes in transport simulation, shelf life, and mechanical testing with a thorough understanding of ASTM, ISTA, and ISO protocols for package integrity testing. Dr. Modi participated in the technical review committee for International Safe Transit Association (ISTA) and a member of Institute of Packaging Professionals (IoPP) and the Association for the Advancement of Medical.