Cost, minimum order, timelines, formula ownership, testing and regulatory questions, answered.
Guires Cosmetic Science Lab
Answers to the questions brands ask Guires CSL most often: what cosmetic development costs, minimum order quantities, timelines, who owns the formula, how NDAs work, which tests and clinical studies a product needs, and how we prepare files for MoCRA, the EU CPSR and other markets.
Start your project with Guires CSLGetting started
It depends on the product type, the number of actives, the claims and the markets. After a short brief call we give a fixed quote for formulation, and separate quotes for testing and regulatory work so you only pay for what you need.
A full project typically takes 21 to 36 weeks from brief to pilot batch. Stability testing and claims studies usually set the pace, and projects that start with an existing formula are shorter.
A short brief: product type, target consumer, a benchmark if you have one, the claims you want, your markets, pack and target price. See the checklist on How we work.
A scientist replies within one working day with next steps and an indicative scope.
Yes, before you share your brief or formula.
Yes. Many first-time founders come to us with an idea and a price point. See the Startups page.
Cost & commercial terms
Fixed fees per stage, agreed in a written proposal. No hidden costs for sample rounds included in the proposal.
Micro-batches are sized to your requirement. There is no factory MOQ.
You do.
Yes. We provide a full tech-transfer pack.
Timelines
Typically 5–9 months from brief to launch-ready, depending on testing, claims and markets. Use the timeline calculator on How we work.
Accelerated stability gives a first read at about 12 weeks; real-time studies continue to confirm shelf life.
Yes. Claims studies and regulatory preparation usually run alongside stability testing.
Testing & claims
At minimum a dermatologist-supervised patch test or in-use study on the final formula. See the claim finder.
No. We use validated in vitro methods, ingredient safety data and supervised human studies.
A preservative efficacy test to ISO 11930 showing the product resists contamination during use.
Regulatory
Yes, through an EU- or UK-established legal entity named in your agreement.
Most brands selling in the US must register facilities and list products. Some small businesses are exempt. Read our MoCRA guide.
An EU-format CPSR is the strongest base; we add market-specific documents.
We prepare the documents needed to obtain Free Sale Certificates and other export papers.
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.