Developing Documents and Records to meet ISO 17025 Requirements 2016

  • 07-08 Jul 2016
  • Tampa, FL, United States

Description

Topics
  • 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

Important

Please, check "Developing Documents and Records to meet ISO 17025 Requirements" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical laboratories
Science: Laboratories, Life Sciences & Biology

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