来自MSN18 天
FDA 510(K) Approved Facilities: Increasing GMP Inspections And Compliance Requirements
Indian medical device manufacturers are prioritizing GMP compliance to meet rising global healthcare demands. Success in inspections requires proactive planning, strong management commitment ...
Forbes1 个月
Are The FDA’s New Regulations On Medical Devices Making A Difference?
In 2023, the Food and Drug Administration (FDA) took a more active approach to medical device cybersecurity. They issued new requirements for premarket submission and ongoing monitoring by medical ...