It’s critical for companies, especially medical device companies, to evaluate their systems and processes to ensure collaboration across their teams and supply chain partners.
With material shortages, plant shutdowns, economic unrest, and increasing natural disasters, how do medical device manufacturers get safe products to market quickly? Coordinating the efforts of multiple teams, often spread across the globe, can be a daunting task even under normal circumstances. When business is disrupted, companies must take quick steps to ensure that product work continues in a fast, efficient, and compliant manner. A product-centric approach to quality management can help optimize processes across all teams and ensure commercialization and compliance success. Hear from a panel of industry experts with in-depth experience bringing FDA-regulated products to market and know what’s needed to meet product development, quality, and compliance goals despite today’s obstacles.