Most of the focus on a laboratory's compliance to Good Laboratory Practice (GLP) or to the analogous ISO 17025 is on items such as the Standard Operating Procedures, training, quality assurance testing, and the statistical assessment of performance and compliance/ These, however, are not all that an auditor may delve into. These might the bulk of an audit, yet a laboratory may fail an audit. Since laboratories focus on them, they might ignore more mundane and simple areas, such as recordkeeping and archiving, basic laboratory operations, and safety.
Why should you attend:
An auditor can find numerous common errors and many, many others that are specific. This seminar will go through many of the compliance areas and point out some of both types. IFor those implementing GLP or striving to maintain certification, this course should point out many areas to cover that would lessen an unsatisfactory audit.
Speaker
John Fetzer
Founder and Principal, Consultant Fetzpahs Consulting (510) 724-8629
John C. Fetzer has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers onl iquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
Please fill in your name and email to receive the seminar agenda of this event.
Time: 9:00 AM to 6:00 PM
The agenda is available as PDF under downloads at the right side of the page.
Venue
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Who will benefit:
Chemists and laboratory assistants who perform HPLC or UPLC analyses under GLP or ISO 17025Chemists and laboratory assistants who perform HPLC or UPLC analyses under GLP or ISO 17025
Venue
DoubleTree by Hilton Hotel San Francisco Airport835 Airport Blvd.
Burlingame CA
