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Event/Course & Registration

627-16SS Document and Record Control

April 21, 2016 — December 31, 2019

Location:


Available April 21, 2016 – December 31, 2019

CEUs not available for this program.

This program is available the day after the live program and is accessible 24 hours a day, 7 days a week!

REGISTER YOUR SITE NOW! FREE/site includes unlimited access for everyone at your site. 

Description
Many laboratory professionals are confused as to what the difference is between a “document” and a “record” and why the laboratory must spend so much time maintaining them. ISO/IEC 17025:2005 has different requirements for documents and records in the laboratory. This presentation will briefly outline those requirements, the subtle differences between a document and a record in the world of Laboratory Quality Assurance, and why they are so important.

Objectives
At the conclusion of this program, the participant will be able to:

  • Discuss why document and record control is important
  • Explain the basic ISO/IEC 17025:2005 standard accreditation requirements for document and record control
  • Define the difference between documents and records in the laboratory

Faculty
Valerie A. Knox, CMQ/OE
Quality System Manager
Food and Drug Administration (FDA)
Jefferson, AR

Additional Information
Registration deadline: December 31, 2019

Problems Registering? Please email registrar@aphl.org or call 240.485.2727 between 8:00 am – 4:30 pm ET.

REGISTER YOUR SITE NOW!

Click here for a complete list of available webinars and archived webinars.

Sessions
There are no additional sessions for this event.