How do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?
Become accredited? Where do you start?
Maintaining the QMS and providing evidence of compliance
Developing and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs
Who should Attend
Attendees from:
Laboratory Quality Development
Laboratory Management/Supervision
Laboratory Quality Control
Laboratory Quality Management
Analytical Support
Past Events
Developing Documents and Records to meet the Requirement of ISO 17025 - 2016 - 20-21 Oct 2016, DoubleTree by Hilton Hotel San Francisco Airport, Burlingame, California, United States (61863)
Developing Documents and Records to meet the Requirement of ISO 17025 2026
Important
Please, check "Developing Documents and Records to meet the Requirement of ISO 17025" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Medical laboratories, Medical technology
