Customer focus
Need certificates, a quality questionnaire completed or an audit of how your project is run? The Guires CSL quality team supports your due diligence and supplier approval.
Quality & accreditations
How Guires CSL controls quality from raw material to finished batch: ISO 9001 certified, with ISO 22716 GMP, ISO/IEC 17025, GLP and GCP standards applied across our work.
Guires Cosmetic Science Lab
Quality at Guires CSL starts at the bench and runs through every batch: a certified quality management system, documented methods, calibrated instruments, traceable raw materials and controlled records, so every result we report can be checked and defended.
Start your project with Guires CSLRaw materials
Every formula is only as good as what goes into it. Guires CSL qualifies suppliers before their materials reach the bench, checks each lot against its specification and certificate of analysis, and keeps raw materials in a controlled store with quarantine and release status.

Testing
Results are only useful if they can be repeated and defended. Guires CSL runs documented methods to ISO and OECD standards on calibrated, maintained instruments, with controls in every run and raw data kept for review.

Pilot manufacturing
Pilot and small batches follow ISO 22716 cosmetic GMP guidelines and the process signed off in development. Each batch is recorded, sampled and checked against its release specification before it leaves the Guires R&D Innovation Centre.

Our people
Quality is part of how the Guires CSL team works, not a final check. Formulation scientists, analysts, microbiologists, toxicologists and regulatory specialists are trained on the procedures they use, and every report is reviewed before it reaches you.

Certificates & standards
| Standard | What it covers | How Guires CSL applies it |
|---|---|---|
| Quality management · ISO 9001 | The quality management system that covers Guires CSL development, testing and project work. | Certified · certificate no. H3CR9TCU20251212INDQM10N |
| Cosmetic GMP · ISO 22716 | Good Manufacturing Practice guidelines for cosmetics, applied to pilot and small-batch manufacturing. | Applied to every pilot batch |
| Testing competence · ISO/IEC 17025 | The general requirements for testing laboratories, applied to the methods on our Testing page. | Scope documents on request |
| Good Laboratory Practice (GLP) | Principles for planning, recording and reporting non-clinical and in vitro studies. | Applied to non-clinical studies |
| Good Clinical Practice & ethics review | GCP for every human study, with independent ethics committee approval before a study starts. | Every clinical study |
Certificates, scope documents and quality policies are available on request.
Support
Need certificates, a quality questionnaire completed or an audit of how your project is run? The Guires CSL quality team supports your due diligence and supplier approval.
Rules differ by market and change often. Guires CSL regulatory specialists link test data to the safety files, claims and labels each market expects, from the EU CPSR to MoCRA.
Every human study runs to Good Clinical Practice, with independent ethics committee approval, informed consent and dermatologist supervision where the study design calls for it.
Certifications we support
Formula and supplier documentation for vegan certification schemes.
Supplier declarations and supply-chain files for cruelty-free certification.
Natural and organic formulation to COSMOS standards, with the files certifiers ask for.
Raw-material tracing and files for your halal certifier.
Case studies
Case studies are published with client permission. Client and product names are withheld under NDA.


Start a project
Our formulation chemists, testing scientists and regulatory specialists work alongside your team, from the first brief to a market-ready product. Bring a brief, a benchmark or just an idea: a scientist will reply within one working day with next steps and an indicative scope.