<< Previous article
Validation of Moist ...
Next article > >
FDA New Endotoxin Te...

ISO/IEC 17025:2017 Section 7 - Process Requirements and Section 8

: 20 Jun 2019

Sector: Clinical, Pharmaceutical

Type: Webinar


Many laboratories have successfully developed and implemented a functional quality management system based on the requirements of ISO/IEC 17025:2005.  Some are still struggling to get accredited and even those already accredited still have issues as evidenced by the number of non-conformances cited during the subsequent biannual audits.

 

A new version of this standard was released on November 19, 2017.  Have the rules changed? What is new and/or different with ISO/IEC 17015:2017? How does the new standard impact upon laboratories that are already accredited? and how can you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits? 

 

Speaker Profile: Michael Brodskyhas been an Environmental Microbiologist for more than 41 years. He is a Past President of the Ontario Food Protection Association and AOAC International.

 

Event Fee: One Dial-in One Attendee Price: $150.00

 

Find out more / register here:

Venue


Organizer

Compliance4All
Phone: +1-800-447-9407
Email: support@compliance4All.com
Visit: http://www.compliance4all.com/control/main


<< Previous article
Validation of Moist ...
Next article > >
FDA New Endotoxin Te...