Webinar: Ensuring ISO 17025:2017 compliance in your Laboratory

A cornerstone of the ISO 17025 Standard is the requirement for laboratories to demonstrate they operate competently and are able to generate valid results. This, in turn, is key to building trust in the quality of the data and information provided to partners, customers and collaborators.

While the 2017 update to ISO 17025 emphasizes a risk-based approach over prescribed working practices, it is still a management system that must be defined, implemented and shown to be adhered to.

This webinar will be held on:
Wednesday 12th June, 2019
8am PDT, 11am EDT USA, 4pm UK, 5pm Europe

The Webinar discusses how a well implemented Laboratory Information Management System can support many aspects of an ISO/IEC 17025:2017 based management system, over and above just the technical records (Section 7.5). It will illustrate how workflow definition and process enforcement aid adherence to an ISO/IEC 17025:2017 management system and discusses the benefits of an integrated information management system strategy.

We will cover a number of aspects of how LIMS supports ISO 17025, among them;

• Data Integrity/Result Validity
• Measurement Uncertainty and Limits
• Instrument Calibration and Maintenance
• SOP and document management
• CAPA management
• Monitoring of environmental conditions for potential contamination

Sign up today to discover how a LIMS can help your Laboratory meet the needs of 17025:2017

Updated: Register to download free copy of the webinar

Simon Wood PhD, has 30 years’ experience of testing and QA compliance in highly regulated industries. An acknowledged expert in the field of scientific and laboratory informatics in the commercial Laboratory Information Management Systems (LIMS) environment he has experience implementing a wide variety of software driven solutions.

As Product Manager at Autoscribe Informatics, Simon uses his considerable experience of international markets to drive development of Matrix Gemini LIMS.