In-service verification of sterilization process
BUSINESS CHALLENGE
Sterilization processes require periodic validation to demonstrate that they are working correctly and functioning within established norms. Such validation entails detailed measuring of various physical parameters throughout the sterilization process and assessing and comparing these results to relevant international standards. To ensure end-users, which include hospitals, clinics and care institutions, the seal of approval must be issued by a qualified entity with worldwide recognition.
Bureau Veritas is a leading partner of choice with a 15-year track record of performing global sterilization process validation.
SOLUTION
Bureau Veritas validates the following processes:
- Steam sterilizers (EN285, NEN-EN-ISO17665-1, prEN13060);
- Hot air sterilizers, including infrared sterilisation (NEN-EN-ISO11138, R6111);
- Ethylene oxide sterilizers (NEN-EN-ISO11135-1).
Under its EN45004 accreditation, Bureau Veritas can also perform validations in accordance with the end-user’s Standard Operating Procedures (SOPs).
WHY CHOOSE BUREAU VERITAS?
- Recognition - Founded in 1828, Bureau Veritas is the worldwide leader in QHSE and Social Responsibility services. Certified to ISO 9001 for all of its worldwide activities, Bureau Veritas actively works with professional authorities, helping to develop international standards and regulations.
- Network - With a network of 1,600 offices and laboratories and over 80,000 employees in more than 140 countries, Bureau Veritas serves 400,000 customers across many different industries worldwide.
- Expertise - All measurements and samplings are performed by experienced technicians and in line with the latest standards and procedures.