2-Day Virtual Seminar Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus) When: Monday & Tuesday Nov 8 - Nov 9, 2021 DAY 01 & Day 02 (9:30 AM TO 5:30 PM)
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.
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 record keeping and archiving.
Register soon because space is limited.
We hope you’re able to join us!