Medical Device Package Testing: Designing a Test Plan to Handle Rigors of Global Supply Chain

Designing a Test Plan to Handle Rigors of Global Supply Chain

With the globalization of the medical device industry, supply chains are getting more rigorous and constantly adapting to the fast-changing distribution environment. The three key challenges to overcome are understanding the global supply chain process, designing safe, protective packaging systems to withstand a multitude of shipping and transportation conditions, and lastly is developing a packaging performance test plan compliant with FDA and/or international health and safety.

We will share insights and a sample test plan focusing on the packaging of medical devices to optimize your time and avoid product development delays. You’ll learn: 

• Overview of various testing standards required to get medical devices to market.
• Testing to consider for various shipping methods
• The status and expectations of the FDA and international agencies.
• How to design a test plan to meet supply chain rigors.

Who should attend?

Managers, directors, engineers, and scientists responsible for research and development, product development, quality assurance, and regulatory compliance. Additionally, procurement, business leaders, and project management personnel responsible for requesting testing quotations.