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Good Laboratory Practice (GLP)

Course Library

A complete library for all of your good laboratory practice needs.

Good Laboratory Practice (GLP) online training courses will help your team easily and conveniently navigate the federal requirements and international guidance for nonclinical laboratory studies.

OSI makes compliance easy for companies in need of GLP introductory and refresher training. Eight GLP courses are available in the OSI library.

Our courses are delivered via a state-of-the-art learning management system that allows you to customize curricula, adjust testing parameters, and even customize courses with site-specific content and photos.

Chemical Facility Security Course Descriptions

252 GLP: Regulations

GLP: Regulations explores the FDA regulation 21 CFR 58 (Good Laboratory Practice for Nonclinical Studies) and two similarly applicable EPA regulations (40 CFR 169 and 40 CFR 792).This course outlines the quality issues addressed in a GLP program, including personnel and training, equipment operation, facility design, handling of test samples, non-clinical studies, and documentation and reporting. (60 mins)

253 Introduction to Good Laboratory Practice (GLP)

Introduction to Good Laboratory Practice (GLP) is an overview course that explains good laboratory practices and their purpose.The course also examines GLP regulations in detail and the fundamentals of GLP. (20 mins)

254 GLP: Resources

GLP: Resources explores the required resources for a nonclinical laboratory study conducted according to good laboratory practice (GLP) regulations.Personnel, facilities, and equipment are discussed in detail. (20 mins)

255 GLP: Responsibilities

GLP: Responsibilities examines responsibilities mandated by 21 CFR 58 “Good Laboratory Practice for Nonclinical Studies” as they apply to testing facility management, the study director, study personnel, study sponsor, and the quality assurance unit.(20 mins)

256 GLP: Conducting the Study

GLP: Conducting the Study examines the conduct of nonclinical laboratory studies according to 21 CFR 58 “Good Laboratory Practice for Nonclinical Studies,” specifically the purpose and use of protocols and standard operating procedures.

257 GLP: Test Articles and Test Systems

GLP: Test Articles and Test Systems provides an overview of the characterization, special handling, and documentation requirements for test articles, control articles, and test systems to achieve good laboratory practices.(30 mins)

258 GLP: Records, Reports and Archives

GLP: Records, Reports and Archives explains how to prepare for a data audit by creating compliant records.This course discusses how to compile these records into a final report for submission to the FDA and how these records must be archived. (25 mins)

259 GLP: Electronic Records, Electronic Signatures

GLP: Electronic Records, Electronic Signatures explains which records fall under 21 CFR Part 11, the characteristics that electronic records must have to be acceptable, and how to control computer systems used to manage electronic records.The course also discusses the types of electronic signatures that are acceptable and the safeguards that must be used so that they will be non-refutable. (30 mins)