Services

UK cosmetic compliance services from safety evidence to market notification.

Each service can be commissioned separately, but the most reliable route is an integrated assessment that keeps the formula, CPSR, PIF, label and SCPN record consistent.

UK Responsible Person

Pretty Yeppuda UK Ltd can act as the appointed Responsible Person for cosmetic products made available in Great Britain, subject to successful completion of our compliance review and a written mandate.

Cosmetic Product Safety Report (CPSR)

We prepare the technical safety-assessment dossier and coordinate signature by an appropriately qualified safety assessor. The assessment considers the qualitative and quantitative formula, toxicological profiles, exposure, intended use, warnings, impurities, packaging and available test evidence.

Product Information File (PIF)

We compile and maintain the product documentation required to substantiate safety, manufacture, claims and regulatory compliance. The PIF is controlled as a living regulatory file and updated when the product, evidence or legal framework changes.

SCPN notification

Before a cosmetic product is first placed on the Great Britain market, the required information is submitted through the UK Submit Cosmetic Product Notifications service. We prepare and manage the notification for products under our Responsible Person mandate.

Ingredient and formulation compliance

Review includes ingredient identity, applicable prohibitions and restrictions, colourants, preservatives, UV filters, nanomaterials, allergens where relevant, impurity concerns and consistency between the formulation and supporting raw-material documentation.

UK cosmetic label review

Artwork is checked for required responsible person details, country of origin where applicable, nominal content, durability or PAO, precautions, batch identification, product function, ingredient listing and the substantiation of claims.

Additional technical support

  • Raw-material and SDS documentation review
  • Stability and packaging compatibility planning
  • Microbiological quality and challenge-test planning where applicable
  • Serious undesirable effect and corrective-action support
  • Change-control and annual compliance maintenance