2024 - Navigating Complex Regulations and Complaints to Achieve Quality Compliance for Life Sciences and Medical Devices

As life sciences and medical device manufacturers strive to scale their operations to meet growing demands in a dynamic landscape, their journey can be full of challenges.
One of the most pressing concerns is navigating customer complaints and regulatory requirements. For example, between 2021 and 2023, the top three citations from the US Food and Drug Administration (FDA) for medical devices were related to lack of or inadequate procedures, complaint procedures and nonconforming products.
In this webinar, the attendees will gain insights into:
Understanding compliance challenges and unique complexities facing the industry such as MedWatch, the FDA’s medical product safety reporting program
Leveraging an enterprise quality management system (EQMS) for best practices for navigating regulatory challenges and streamlining complaints management while scaling operations to mitigate risk
Lessons learned along the way of achieving successful compliance
Register for this webinar today to gain invaluable insights into overcoming quality compliance challenges in the life sciences and medical device industries.
Keywords: Quality Control, Medical Device, Regulatory, Regulatory Compliance, Quality Assurance, Medical Device Regulation, Quality Management, Medical Device Manufacturing, Commercial Manufacturing, Quality Compliance, Quality Management System, QMS, CDMO/CMO, Quality