Cosmetic Product Information File (PIF)
Bring the product documentation together in a structured file your EU Responsible Person can maintain and make available to authorities.
What we handle
- Compilation of the Product Information File from the required product documents.
- Identification of missing documentation needed to complete the agreed file.
What we need from you
- Product description, final formula and packaging/label artwork.
- Existing CPSR, manufacturing method and GMP information.
- Claims substantiation, available test reports and relevant animal-testing information.
Scope boundaries
- CPSR preparation and new laboratory tests are not included in the PIF compilation fee.
- The file must remain accessible through the EU Responsible Person and be updated when relevant product information changes.
From enquiry to deliverable
Confirm the product and scope
Tell us what you sell, where it will be sold and what evidence is already available. If you are unsure, contact us before ordering.
Submit the intake and pay securely
The application leads to Stripe Checkout for this exact service in EUR. Send the listed documents to info@fdabridge.com; do not send samples without instructions.
Receive the agreed work
We review document completeness, coordinate the assessment or testing and deliver the agreed report or file. Any additional scope is explained before further work.
Does this fee include the CPSR?
No. The CPSR is part of a complete PIF, but preparing a new CPSR is a separately priced service. Send your existing report if you have one.
Official background: European Commission: EU cosmetics legislation. FDABridge is an independent private provider. Assessment, review and notification are not government approval.