Ensuring Patient Safety: A Deep Dive into EU MDR/IVDR Article 10a
Patient safety remains a cornerstone of the global medical device industry, and the European Union is taking significant steps to uphold this principle. With the introduction of Article 10a under the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), manufacturers must proactively address potential supply interruptions that could jeopardize patient care. Effective January…