627-16SS Document and Record Control
April 21, 2016 December 31, 2019
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!
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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.
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
Valerie A. Knox, CMQ/OE
Quality System Manager
Food and Drug Administration (FDA)
Registration deadline: December 31, 2019
Problems Registering? Please email email@example.com or call 240.485.2727 between 8:00 am – 4:30 pm ET.
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There are no additional sessions for this event.