GLP Good Laboratory Practice Practice Test

The GLP Good Laboratory Practice Practice Test is a free intermediate-level, 20-minute skill test from Science of Apps. It tests Good Laboratory Practice (GLP) knowledge — GLP principles, scope and mutual acceptance of data, test facility organisation with the roles of management, the Study Director and Quality Assurance, study conduct, test systems, test items and facilities, and records, data integrity, reporting and archiving — written to the OECD Principles of GLP, US FDA 21 CFR Part 58 and UK MHRA GLP guidance for 2026. Score 70% or more on its 20 questions to earn a verifiable GLP Good Laboratory Practice Readiness certificate (SOA-GLPG). Every question is based on published standards and research — including OECD Principles of Good Laboratory Practice and Compliance Monitoring series (incl. Mutual Acceptance of Data) (OECD), 21 CFR Part 58: Good Laboratory Practice for nonclinical laboratory studies (US FDA (eCFR)), Good laboratory practice (GLP) for safety tests on chemicals (UK MHRA (GLP Monitoring Authority)) — and each answer is explained with its source.

Yes. Science of Apps has a free GLP Good Laboratory Practice Practice Test built on the current exam outline for 2026 and 2027. It covers GLP principles and scope, roles and organisation, study conduct, test systems and facilities and records, data integrity, reporting and archiving, scores you instantly and issues a verifiable certificate.

Read the four skill areas on this page, then take the 20-minute test online — no fee, course or sign-up. You see every answer explained when you finish. Score 70% or more and you get a GLP Good Laboratory Practice Readiness certificate straight away, on screen, as a PDF and by email, with a credential ID anyone can verify.

Yes. The questions are original scenarios written by Science of Apps, and each one is based on a public source you can read: OECD Principles of Good Laboratory Practice and Compliance Monitoring series (incl. Mutual Acceptance of Data) (OECD); 21 CFR Part 58: Good Laboratory Practice for nonclinical laboratory studies (US FDA (eCFR)); Good laboratory practice (GLP) for safety tests on chemicals (UK MHRA (GLP Monitoring Authority)); Part 11, Electronic Records; Electronic Signatures (US Food and Drug Administration). The source is shown under each question and linked in the answer review. Science of Apps doesn't copy questions from other tests.

Four skill areas with five questions each, drawn from a bank of 10 per area so a retake brings new questions: GLP Principles and Scope (Purpose of GLP, Scope of application and Mutual acceptance of data); Roles and Organisation (Test facility management, Study Director and Principal Investigator and Quality Assurance); Study Conduct, Test Systems and Facilities (Study plans and SOPs, Test items and test systems and Equipment and facilities); Records, Data Integrity, Reporting and Archiving (Raw data and corrections, ALCOA+ and Final report and archives). Every question is an original scenario written to the 2026–2027 standard, with the published source named under it.

Laboratory scientist or technician in non-clinical safety studies, Study Director, Quality Assurance auditor, Toxicology or CRO staff and Laboratory archivist. It suits anyone who wants a quick, verifiable way to show GLP Good Laboratory Practice knowledge in 2026 and 2027, from students and career switchers to experienced professionals.

GLP is a quality system for how non-clinical health and environmental safety studies — such as toxicology studies supporting the approval of medicines, pesticides and chemicals — are planned, performed, monitored, recorded, reported and archived. It makes study data reliable and traceable so regulators can accept it.

No. GLP covers non-clinical safety studies. Clinical trials in people follow Good Clinical Practice (ICH E6), and manufacturing follows Good Manufacturing Practice (GMP).

Yes. The test is online, in English and free everywhere — people take it from India, the US, the UK, Europe, Africa, Latin America and Asia-Pacific. Your certificate is dated with your own local date and can be verified from anywhere at scienceofapps.com/certification/verify/.

20 questions — 5 from each of 4 skill areas — with a 20-minute limit. You need 70% (14 of 20) to pass and 90% for distinction.

We rate it Intermediate: assumes hands-on experience in the role. It has 20 scenario questions — 5 from each of 4 skill areas — and a 20-minute limit. You need 70% (14 of 20) to pass and 90% for distinction.

Nothing. There is no fee to take a test, to receive the certificate, to have it emailed or to verify it, and no sign-up.

On our server, not in your browser. The answers never reach the page until you submit, so a certificate can only be earned by passing. Each certificate gets a unique credential ID stored by Science of Apps.

You see your score for each area and every question with the correct answer and why, with the published source behind it. You can retake after 30 minutes, and the retake draws questions you haven't seen yet.

No. Every certificate is dated, so it always shows when you passed. Retake a test any time for a newer date or a higher score.

Yes. After you pass, Add to LinkedIn opens the Licenses & certifications form with the certificate name, Science of Apps as the issuer, the issue date, your credential ID and the verification link filled in. You can also download it as a PDF or PNG, and it's emailed to you as a PDF.

Every certificate has a credential ID and a QR code. Scanning it, or entering the ID at scienceofapps.com/certification/verify/, shows the holder's name, the certification, the score and the issue date from our records.

No. They are Science of Apps' own assessments of applied skill. They aren't issued by a university or standards body, and they work best alongside a portfolio that shows the skills in real work.