This webinar addressed the pressing need for standardized regulatory practices in the field of in vitro diagnostics (IVDs) as advancements are made in an increasingly interconnected global healthcare landscape and demand grows for more precise diagnostics.
The consequences discussed in terms of their effects on regulatory complexity, patient safety, innovation and access, global collaboration, and early-career professionals. This topic should be of special interest to those in such roles as laboratory managers, technicians, healthcare providers, regulatory professionals, researchers, and industry experts in need of IVD-related critical tools to enhance compliance, streamline operations, and foster innovation in laboratory medicine, ultimately improving patient care and advancing the field.
Upon completion of this continuing education program, participants should be able to:
Understand the significance of regulatory harmonization in IVD.
Identify common challenges and pain points.
Gain access to valuable resources for ongoing learning.
