Comprehensive online GLP Internal Auditor training aligned with MHRA requirements, the Good Laboratory Practice Regulations 1999, OECD Principles of GLP, and ISO 19011 auditing standards — trusted by UK pharmaceutical, chemical, and biotechnology professionals. Self paced. 21 CFR Part 11 compliant certificates. Inspection ready training records.
The United Kingdom has a comprehensive regulatory framework for Good Laboratory Practice (GLP) that is based on the OECD Principles of GLP and implemented through the Good Laboratory Practice Regulations 1999 (SI 3106) . The Good Laboratory Practice Monitoring Authority (GLPMA), part of the Medicines and Healthcare products Regulatory Agency (MHRA), is responsible for administering the UK GLP Compliance Monitoring Programme.
Key Regulatory Frameworks:
The Good Laboratory Practice Regulations 1999 apply to those test facilities that conduct or intend to conduct a regulatory study
Laboratories and other facilities that do regulatory studies are subject to routine biennial inspection
Membership of the GLP compliance programme is mandatory for such organisations
All work must be done in accordance with the principles of GLP
| Regulatory Authority | Framework | Application |
|---|---|---|
| MHRA | Good Laboratory Practice Regulations 1999 (SI 3106) | UK implementation of OECD GLP Principles |
| MHRA | GLP Compliance Monitoring Programme | Routine biennial inspections of test facilities |
| OECD | OECD Principles of GLP (as revised in 1997) | Mutual Acceptance of Data (MAD) |
| European Union (applicable) | Directives 2004/9/EC and 2004/10/EC | EU GLP framework (applicable where retained) |
All courses are self paced, available online, and include 21 CFR Part 11 compliant certificates with verifiable IDs — accepted as documented training records during EMA, MHRA, and other regulatory inspections.
This training program defines the complete knowledge and performance requirements for personnel within a nonclinical laboratory testing facility to become certified internal auditors for Good Laboratory Practice (GLP) as prescribed in the OECD Principles of Good Laboratory Practice (as revised in 1997). The program integrates GLP requirements for single site and multi site studies with internal auditing practices based on ISO 19011. The participant learns both what the OECD GLP requires and how to plan, execute, report on, and close internal audits of those requirements.
This comprehensive training program offers an in depth examination of the OECD Principles of Good Laboratory Practice (GLP), as revised in 1997. Tailored for professionals in the pharmaceutical, chemical, and biotechnology sectors, the curriculum addresses the complete range of GLP requirements, including organizational responsibilities, quality assurance, study conduct, data integrity, and archival management.
The program equips participants with practical knowledge of how GLP facilitates the production of reliable, reproducible, and internationally recognized non clinical safety data, thereby supporting regulatory compliance, safeguarding human health, and enabling the Mutual Acceptance of Data (MAD) in global markets.
Enroll in Good Laboratory Practices (OECD Focused)This self study training program defines the complete knowledge and performance requirements for personnel within a nonclinical laboratory testing facility to become certified internal auditors for Good Laboratory Practice (GLP) as prescribed in 21 CFR Part 58. The program integrates GLP requirements for nonclinical laboratory studies with internal auditing practices based on ISO 19011.
Enroll in GLP Internal Auditor Certification (OECD Focused)This comprehensive training program is designed to provide individuals with a thorough understanding of ISO 19011:2026, "Guidelines for Auditing Management Systems." The program covers all aspects of the standard, including the principles of auditing, managing an audit programme, conducting management system audits, and evaluating the competence of individuals involved in the audit process.
Enroll in ISO 19011:2026GLP Auditor Certification is a legal requirement for personnel responsible for auditing nonclinical laboratory testing facilities.
The Good Laboratory Practice Monitoring Authority (GLPMA), part of the MHRA, is responsible for administering the UK GLP Compliance Monitoring Programme. Laboratories and other facilities that do regulatory studies are subject to routine biennial inspection. Inspection findings can have serious consequences:
| Feature | GxP Trainings |
|---|---|
| Good Laboratory Practice Regulations 1999 aligned | |
| MHRA GLP Compliance Monitoring Programme aligned | |
| OECD Principles of GLP aligned | |
| 21 CFR Part 58 (FDA GLP) covered | |
| ISO 19011 auditing principles covered | |
| 21 CFR Part 11 compliant certificate | |
| Self paced — study on your schedule | |
| Instant certificate download | |
| Verifiable certificate ID | |
| Group / corporate enrollment |
Yes. The MHRA does not mandate a specific training delivery format. What matters is that training is documented, role appropriate, and effective. Our 21 CFR Part 11 compliant certificates provide verifiable proof of training that MHRA inspectors accept during inspections.
The UK GLP Compliance Monitoring Programme is administered by the GLPMA (part of the MHRA) and involves routine biennial inspections of laboratories and other facilities that conduct regulatory studies. Membership of the programme is mandatory for such organisations.
The OECD Focused course is based on the OECD Principles of GLP (as revised in 1997), which form the basis for UK GLP requirements. The FDA Focused course is based on 21 CFR Part 58, which is specific to FDA requirements. Both courses provide comprehensive internal auditor training.
Completion of basic GLP awareness training of at least four hours or equivalent on the job experience, and at least six months of experience in a nonclinical laboratory testing facility.
We offer corporate and group enrollment options for teams of all sizes. Contact us for a custom quote.
All courses include lifetime access — study at your own pace, on your own schedule.
Yes. Each certificate includes a unique verifiable ID that can be checked at gxptrainings.com/verify-certificate/
Equip yourself and your team with the GLP knowledge and documented training records required for MHRA, EMA, and FDA inspection readiness.