Process Validation: Pharma vs. Medical Device

Process validation difference between Pharma vs. Medical Device industries

RS-NESS provides an umbrella of services to the Life Science industry in the areas of validation, quality assurance, regulatory affairs, clinical affairs, project management, and engineering. This approach enables a “one-stop-shop”, incorporating end-to-end project activities while adhering to the regulatory requirements. Knowledge, professionalism, and dedication lead our highly qualified team to your success.

MDSAP In 60 Sec

Medical Device Single Audit Program (MDSAP) in 60 Sec | RS NESS

For those who are not familiar with the Medical Device Single Audit Program (MDSAP), it is a harmonized approach for auditing and monitoring medical device manufacturers quality management system on an international scale. MDSAP program allows a single regulatory audit of a medical device manufacturer’s quality management system to satisfy the needs of participating regulatory […]