Netzealous LLC DBA - Compliance4All, Online
2017-10-04
Overview: Good Laboratory Practice (GLP) is a quality system which intend for non-
clinical studies and was revised by several bodies. GLP is a unique quality
system in the sense it is intend for non-routine processes and activities.
Why should you Attend: The authorities often required a GLP declaration and statement for submitted
studies. Come to hear more on the requirements and particularly if you
moving from another quality system like GMP or ISO 17025 to GLP, make the
differences between these quality systems clear and prevent confusing
especially if they are coexist in your site.
Areas Covered in the Session: The Role and Responsibilities of the Study Director in GLP Studies The Role and Responsibilities of the Sponsor in the Application of the
Principles of GLP Terms/Vocabulary FDA GLP 21CFR 58 EPA GLP
Who Will Benefit: Study Directors Laboratory Managers R&D Researchers of Pharmaceutical and Veterinary Companies Quality Control Staff Regulatory Affairs (RA) Staff
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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