DESCRIPTION GLP requires many types of documents. The seminar covers both the general issues and many specifics that laboratories can receive a non-compliance on. These range from data recording to validation issues to training records to archiving of documents. An auditor can find numerous common errors and many, many others that are specific to a particular laboratory. This seminar will go through many of the compliance areas and point out some of both of these types. For those implementing GLP or striving to maintain certification, this course should point out many areas to examine that would lessen an unsatisfactory audit. Most of the

Date : 14th December 2017 to 15th December 2017

Place : United States, San diego

Website :https://www.eventbrite.com/e/recordkeeping-and-documentation-in-a-glp-laboratory-us-fda-us-epa-and-osha-focus-com-a-tickets-37334598790?aff=NDT

Contact Person:Paula Edwards

Description:

DESCRIPTION GLP requires many types of documents. The seminar covers both the general issues and many specifics that laboratories can receive a non-compliance on. These range from data recording to validation issues to training records to archiving of documents. An auditor can find numerous common errors and many, many others that are specific to a particular laboratory. This seminar will go through many of the compliance areas and point out some of both of these types. For those implementing GLP or striving to maintain certification, this course should point out many areas to examine that would lessen an unsatisfactory audit. Most of the

DESCRIPTION GLP requires many types of documents. The seminar covers both the general issues and many specifics that laboratories can receive a non-compliance on. These range from data recording to validation issues to training records to archiving of documents. An auditor can find numerous common errors and many, many others that are specific to a particular laboratory. This seminar will go through many of the compliance areas and point out some of both of these types. For those implementing GLP or striving to maintain certification, this course should point out many areas to examine that would lessen an unsatisfactory audit. Most of the will be held in San diego,United States on date 2017-12-15

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Deadline for abstracts/proposals : 13th December 2017

Keynote Speakers : John C. Fetzer, PhD, Consultant, Fetzpahs Consulting Dr. Fetzer has been a method-development analytical chemist for over 3 decades. In that role he developed new methods for GC, HPLC, fluorescence spectroscopy, titrimetry, the use of ion-selective electrodes, and physical properties of aqueous solubility and octanol-water partition coefficient that complied with Good Laboratory practices. As part of his consulting and contracting work he developed GLP-compliant methods for a biopharma start

Conference Highlights :Learning Objectives: Upon completing this course, participants should: -Know the variety of common documentation within a compliant laboratory. -Understand the requirements for entering information into logbooks and also to know some of the ways that are not compliant. -Understand the importance of logbooks for: chemicals, instruments, calibration, maintenance and repair, calibrations, training and competence. Know the information suitable in each type. -Understand the requirements for

Venue :San Diego, CA, United States

Check the event website for more details.