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Drafting and evaluation of cosmetic dossiers (DIP)

For the marketing of a cosmetic product, Regulation 1223/2009 requires the preparation of a Product Information File (DIP), codified and structured around the Cosmetic Product Safety Report (RSPC). The purpose of this dossier is to demonstrate that there is no risk to consumer health. When a cosmetic product is placed on the market within the European Union, the Responsible Person is required to make this Product Information File (PIF) available to the competent authorities. This file must include a product safety assessment validated by a toxicologist.
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Laboratoires Lelégard offers you personalized and flexible support for compiling your Product Information Files (PIFs).

Our services

  • We compile and draft your DIPs in their entirety. Would you prefer to take care of this yourself? In that case, we will take care of the safety assessment report (part 2B). Your file will be brought into compliance with European Cosmetics Regulation 1223/2009.

  • Bringing your DIPs into compliance with the new regulations in force.

  • Update your DIPs following a rebranding, brand acquisition, or business takeover.

  • Centralization of all compliance, efficacy, and safety testing if required for your product. We take care of planning and communication with the relevant laboratories on your behalf.

  • Creation of your account and notification on the CPNP portal (for the European market). The same applies to the OPSS (for the UK market).

  • Regulatory advice on your formulations, packaging, and labeling. We help you draft your labels. This ensures that your claims comply with the «six common criteria.».

regulatory assessment DIP

Our support

The person responsible for placing a cosmetic product on the market within the European Union must provide the competent authorities with a product information file (PIF) comprising five mandatory sections. One of these sections concerns the safety assessment of the product, which must be validated by a toxicologist.

Our multidisciplinary team of toxicologists specializing in regulatory affairs and cosmetics trainers will assist you in drafting and validating your DIPs. We offer a customized service tailored to your needs and will partner with you in carrying out your project by proposing solutions to resolve compliance issues.

In addition, with our 10 years of expertise in formulation, we are able to advise you on bringing your formulas into compliance.

We are committed to offering you reliable and competitive services so that you can bring your products to market as quickly as possible.

Rates for drafting DIPs

Our fees for drafting prospectuses are customized and require a quote, so please do not hesitate to contact us.

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Would you like to know our rates for our service? Drafting and evaluation of cosmetic dossiers (DIP) ?

Quote Drafting and evaluation of cosmetic dossiers (DIP) online

Why use Lelégard Laboratories?

A team of toxicologists specializing in regulatory affairs for the Swiss and European markets.

• We provide comprehensive expertise in formulation, toxicology, and regulatory compliance tailored to organizations of all sizes.
• We support brands at every stage of their cosmetic development with reliable and rigorous technical analyses.
• We secure your projects by guaranteeing the quality, safety, and compliance essential for market launch.

• Creation of DIP/PIFs that comply with current regulatory requirements, whether the European Cosmetics Regulation or the Swiss Cosmetics Ordinance (OCos).

About us

Cosmetic regulatory and toxicology services and training.

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