Good Laboratory Practices (GLP)

No training program is complete without a solid core of comprehensive courses.  Good Laboratory Practice (GLP) online training courses will help your team easily and conveniently navigate the federal requirements and international users_idance for nonclinical laboratory studies.These courses cannot be administered and paid for online by the user, they must be assigned by ASC.  Please click Register buttons to send us a request for these courses and we will contact you shortly to complete transaction and get you started!!!

Courses for Good Laboratory Practices (GLP)

 252 GLP: Regulations

registerExplores 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 also addresses OECD principles, the international counterpart to U.S. regulations.

 253 Introduction to Good Laboratory Practice (GLP

registerIs an overview course that explains GLP and its purpose. The course also examines GLP regulations and the fundamentals of GLP.

 254 GLP: Resources

registerExplores the required resources for a nonclinical laboratory study conducted according to GLP. Personnel, facilities, and equipment are discussed in detail.

 255 GLP: Responsibilities

registerExamines the responsibilities mandated by 21 CFR 58 as they apply to testing facility management, the study director, study personnel, and the quality assurance unit.

 256 GLP: Conducting the Study

registerExamines the conduct of nonclinical laboratory studies according to 21 CFR 58 with special attention to the purpose and use of protocols and standard operating procedures.

 257 GLP: Test Articles and Test Systems

registerProvides an overview of the characterization, special handling, and documentation requirements for test articles, control articles, and test systems.

 258 GLP: Records, Reports, and Archives

registerExplains 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.

 259: Electronic Records, Electronic Signatures

registerExplains which records fall under 21 CFR Part 11 (also known as 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.

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