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

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Category Educational webinars, Healthcare webinars, Biopharmaceutical, Laboratory Managers, pharmaceutical trainings

Deadline: June 18, 2019 | Date: June 20, 2019

Venue/Country: Online, U.S.A

Updated: 2019-04-22 16:17:03 (GMT+9)

Call For Papers - CFP

How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?

Why should you Attend:

What are the changes to the technical and management requirements and how should these be addressed? This webinar will discuss the old as well as the new changes in the standard and their impact on your QMS.

Areas Covered in the Session:

Handling of customer items

Technical records

Evaluation of uncertainty of measurement

Validity of results

Reporting of results

Who Will Benefit:

Laboratory Managers

QA Managers

QC Analysts

College Student

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

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com