--- title: "Good Laboratory Practice Support" description: "Document relevant non-clinical studies under applicable GLP requirements." image: "https://cosmetic-labs.com/wp-content/uploads/glp-documentation-service-1200x1200-1.webp" --- # Good Laboratory Practice Support > Document relevant non-clinical studies under applicable GLP requirements. Source: https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/glp-documentation Created: 2024-12-25T02:04:43+00:00 Modified: 2026-10-25T11:30:03+00:00 Author: Emilie SCHOL Good Laboratory Practice Support | Cosmetic Labs ## What is Good Laboratory Practice Support? GLP documentation records how a study is planned, performed, checked and archived under applicable Good Laboratory Practice requirements. For cosmetic projects, it supports traceability of relevant non-clinical safety studies where GLP is required or specified, rather than certifying every product test. ### Why do you need this service? Use GLP support for applicable nonclinical health or environmental safety studies where the intended use requires that quality framework. Confirm the facility status, study scope and receiving requirements before commissioning work. ## Be the first company on this service page No published company profiles are linked to Good Laboratory Practice Support or its more specific services yet. Explore the service categories or add an explicitly supported capability to your company profile. [List your company](https://cosmetic-labs.com/account/companies/new) Definition ## GLP documentation for relevant cosmetic studies Good Laboratory Practice is a quality system for the organisation and conduct of applicable non-clinical health and environmental safety studies. It is not a universal requirement for every cosmetic efficacy, stability or microbiological test. Confirm the study’s intended regulatory use, applicable framework and facility scope before commissioning GLP work. ### Records across the study An approved study plan and documented amendments or deviations - Identified test and reference items and sample records - Relevant standard operating procedures and equipment records - Contemporaneous raw data with attributable entries - Independent quality-assurance oversight and statements as applicable - A final report and arrangements for archiving supporting records Documentation should show how results were generated and controlled. A collection of certificates produced after testing cannot retrospectively make a non-GLP study GLP-compliant. ### Use in dossiers The study report and relevant supporting records can contribute to a safety assessment or regulatory package where appropriate. The receiving requirements determine what must be supplied and retained. Verify a provider’s GLP compliance status and study coverage rather than relying on an unspecific claim of certification. GLP records do not by themselves prove product safety, satisfy every retailer or replace scientific assessment of whether the method answers the question. Applications ## Applications of GLP support ### Establishing study records An appropriate study plan, identified test items, contemporaneous raw data, documented procedures and independent quality-assurance activities support traceability. Changes and deviations need records under the applicable framework. A later certificate cannot retrospectively turn a non-GLP study into a GLP study. ### Keeping the boundary clear Human patch tests are clinical studies and are not automatically governed by a nonclinical GLP framework. Nor are all cosmetic stability, microbiological or efficacy studies universally subject to FDA 21 CFR Part 58. Retention and submission requirements depend on the framework and use; GLP documentation does not itself prove product safety or general regulatory acceptance. ExplorationLearn more about Submission DocumentationFind technical report translation, traceable submission data preparation and applicable GLP documentation support for defined cosmetic regulatory purposes. Explore another Submission Documentation page on cosmetic-labs.com. #### [Submission data files](https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/raw-data) Prepare traceable study datasets and source records in the recipient’s required format, with links to methods, product versions and supporting reports. [Check this service](https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/raw-data) #### [Technical Report Translation](https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/multi-language) Translate cosmetic study and regulatory reports while preserving technical meaning, with language scope, terminology and review responsibilities defined. [Check this service](https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/multi-language) Continue with [Google](https://cosmetic-labs.com/?lean_auth=start&provider=google&redirect_to=https://cosmetic-labs.com/&error_return=https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/glp-documentation) [LinkedIn](https://cosmetic-labs.com/?lean_auth=start&provider=linkedin&redirect_to=https://cosmetic-labs.com/&error_return=https://cosmetic-labs.com/services/market-access/regulatory-compliance/submission-documentation/glp-documentation) What does “Verified” mean? Verified means the claimant’s company affiliation was checked. Something not right?Let us know if any information on this page is incorrect or if you have concerns about who manages it. [Report an issue](https://cosmetic-labs.com/platform/contact) © 2026 Cosmetic Labs. All rights reserved. --- ## Site identity - Organization: Cosmetic Labs - Description: Cosmetic Labs is a directory and a platform to meet all your cosmetic product development needs. 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