🧼 MDSAP-Certified Decontamination Services: What You Should Know

Medical device safety is a top priority for manufacturers, healthcare providers, and patients alike. One of the critical steps in ensuring that reusable medical devices remain safe and effective is proper decontamination. C.G. Laboratories, an ISO 13485 certified laboratory, offers specialized MDSAP-certified decontamination services designed to support global regulatory compliance and patient safety. In this blog, we explore everything you need to know about these services, why they matter, and how they integrate with broader medical device validation processes.

🔬 What Is an MDSAP-Certified Decontamination Service?

The Medical Device Single Audit Program (MDSAP) allows medical device manufacturers to meet multiple regulatory requirements through a single audit. An MDSAP-certified decontamination service adheres to rigorous international standards, ensuring that the cleaning and decontamination of medical devices comply with FDA, Health Canada, ANVISA, TGA, and Japan’s PMDA regulations.

Visit for more info: https://cg-labs.com