Ensuring Audit Readiness Through Automated Medical Device Document Management Systems The Growing Audit Pressures Facing Life Sciences and Medical Device Manufacturers
Rising regulatory, compliance, and operational expectations
Across the global Life Sciences sector, manufacturers in regions such as the US, UK, Germany, Switzerland, Singapore, and Australia face a rapidly tightening regulatory landscape. The intensity of FDA, MHRA, EU MDR, IVDR, and ISO 13485 requirements...