EN ISO 11737-1 Sterilization of Health Care Products - Microbiological Methods - Determination of Microorganism Population on Products

This standard provides guidance on how to count and characterize microorganisms in healthcare products, helping users to indicate the success of sterilization.

For whom EN ISO 11737-1 is;

• Medical Device Manufacturers
• sterilization service providers
• Other professionals responsible for sterilization
   

A sterile healthcare product is one that is free from live microorganisms. For sterilization to be successful, the presence and nature of bacteria and other microorganisms must be adequately predicted. To this end, this standard provides guidance on the enumeration and microbial characterization of the viable population of microorganisms on or in a health care product, ingredient, raw material, or package.

EN ISO 11737-1 Standard;

• Provides detailed, reliable guidance on bioburden testing
• Supports the use of common terminology in sterilization processes
• Helps increase confidence in your products
• Helps manage risk

EUROLAB assists manufacturers with EN ISO 11737-1 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.