Collaboration Process

Transparency and full control over the project are the foundations of our work. We guide your brand through complex legal procedures step by step, minimizing the risk of errors and optimizing the time-to-market for your cosmetic product.

Here is the path from the initial formulation to legal sales:

1. Initial Consultation and Strategy

We begin every project by securing your know-how through a Non-Disclosure Agreement (NDA). Next, we discuss the specifics of your product, target markets, and launch schedule. We identify any potential gaps in the testing documentation and determine the optimal regulatory pathway.

Document Audit and Analysis

Before we begin drafting the report, we conduct a rigorous audit of the collected data. We verify raw material specifications, Safety Data Sheets (SDS), IFRA certificates, laboratory test results, and planned marketing claims for compliance with current regulations.

3. Preparation of the Cosmetic Product Safety Report (CPSR)

Once the Product Information File (PIF) is complete, we develop the key document: the Cosmetic Product Safety Report (CPSR, Parts A and B). We perform a detailed toxicological assessment and risk analysis, and calculate the Margins of Safety (MoS), guaranteeing the reliability and legality of the formulation.

4. Product Registration and Notification

Once the cosmetic product receives a positive safety assessment, we take over the market compliance process. We execute precise submissions in the required portals and systems (e.g., the European CPNP, the British SCPN, the American MoCRA, or the Middle Eastern SFDA systems).

5. Post-Market Support and Development

Cosmetic regulations are constantly evolving, and our support does not end at registration. We monitor legislative amendments (e.g., bans on new ingredients), prepare necessary updates to CPSR reports, and advise on formulation modifications or during expansion into entirely new markets.