The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: June 26, 2015 from 1pm to 2pm
Street: 5939 Candlebrook Ct
Website or Map: https://compliancetrainings.c…
Event Type: webinar
Organized By: Compliance Trainings
Latest Activity: May 12, 2015
Developing a Quality Management System (QMS) as a prerequisite for getting accredited is relatively easy. Maintaining the QMS to retain your accreditation status is the real challenge and a measure of the robustness your System.
Many laboratories struggle with 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. Once accreditation has been achieved many laboratories have difficulty maintaining the QMS as evidenced by the number of non-conformances cited during the subsequent biannual audits.
Why do you want to become accredited?
Where do you start?
For laboratories that are already accredited, how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits? Getting there is relatively easy. Staying there is hard part.
Areas Covered in the Session :
Defining a Quality Management System (QMS)
Management Components of a QMS
Technical Components of a QMS
Method Selection, Validation and Verification
Ensuring analytical competency
Ensuring analyst competency
Who Will Benefit:
Laboratory Quality Development
Laboratory Quality Management
Laboratory Quality Control
Single Live : For One Participant
Corporate Live : For Max. 10 Participants
Single REC : For One Participant - Unlimited Access for 6 Months
For more information and enquiries contact us at
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : firstname.lastname@example.org
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