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PIF for Perfumes & Fragrances (Including Eau de toilette/parfum, solid perfume, perfumed oils & powders)

PIF for Perfumes & Fragrances (Including Eau de toilette/parfum, solid perfume, perfumed oils & powders)

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Introduction

Fine fragrance PIF for Perfumes & Fragrances documentation places weight on the fragrance composition documentation the IFRA compliance certificate and allergen breakdown — since this underpins both the CPSR conclusion and the ingredient list on your label. Manufacturing documentation covers compounding and, for alcohol-based formats, flammability handling.

What Is a PIF?

A cosmetic product information file is the single evidence file your Responsible Person holds for each cosmetic product, built from your cosmetic product safety report and manufacturing records, and produced on request by a competent authority.

What Your PIF Includes

  • Raw material documentation and CPSR cross-reference
  • Manufacturing method (compounding, maceration, filling) with GMP statement, covering base formulation
  • IFRA compliance certificate and allergen breakdown, held as core supporting evidence
  • Claims substantiation for longevity or sillage claims, where made
  • Animal testing declaration

Who This Is For

Perfumers and fragrance brands maintaining PIF for Perfumes & Fragrances documentation for eau de toilette, eau de parfum, solid perfume or perfumed oils, for cosmetic products sold in the UK and EU.

Legal Framework

  • Article 11, EU Regulation (EC) No 1223/2009
  • Schedule 34, SI 2019/696
  • ISO 22716
  • Annex III
  • Current IFRA Standards

A product information file is required for all cosmetic products and EU markets alike, so a single, correctly structured file meets legal requirements on both sides.

What Do You Need To Provide

Your existing cosmetic product safety data, fragrance concentrate composition, and IFRA certification for the finished blend.

Why Brands Choose Spectra Cosmetic Compliance for Your PIF

  • Built directly from your CPSR, so your safety data and PIF are consistent from day one — no re-entering formulation data, with full safety assessment integration across both documents.
  • GMP documentation reviewed against ISO 22716, the recognised UK/EU cosmetic manufacturing standard.
  • Claims substantiation flagged and structured, covering labelling and claims so "proof of effect" is ready before an authority asks for it.
  • Held to a single, consistent format your Responsible Person can present at inspection without last-minute assembly, keeping your maintaining records obligation straightforward.
  • Retained and managed for the full statutory 10-year period, built from fully compliant PIFs.
  • Every file is tailored to your specific fragrance concentration and format, leaving your product market-ready and compliant.
  • Backed by regulatory information structured specifically for perfumers, not generic cosmetic templates.

Your PIF Deliverables

  • Product description name, category, function and any variant/shade codes, clearly linking the file to your product
  • CPSR (Parts A & B) cross-referenced from your existing safety assessment
  • Manufacturing method description and GMP statement structured to ISO 22716
  • Claims substantiation file evidence behind any effect claimed on your label or marketing, where applicable
  • Animal testing declaration confirming testing status for the product and its ingredients, as required under Article 18
  • Delivered in a single, inspection-ready file, held at your Responsible Person's address

How It Works

  1. Share your CPSR and formulation records if Spectra prepared your CPSR, this step is largely automatic.
  2. We compile the manufacturing and GMP documentation working from your production records or manufacturer's GMP statement.
  3. We structure your claims evidence matching each label or marketing claim to its supporting data.
  4. We confirm your animal testing declaration checked against Article 18 requirements.
  5. You receive your complete PIF, ready to hold at your Responsible Person's address for inspection, via a professional submission process designed to be smooth and professional from start to finish.

Yes this is a key piece of supporting evidence and should be held on file, not just referenced.

Generally yes, since concentration affects the exposure and allergen-labelling conclusion, though the underlying fragrance data can be shared efficiently.

It skips the ethanol flammability handling documentation, but needs the same fragrance composition and allergen evidence.

Your PIF should be updated to hold the current certificate, since an outdated one may not reflect the latest IFRA Standards Amendment.

Yes wear-time or longevity testing evidence proportionate to the claim should be documented in the claims substantiation section.

Yes where relevant to your production process, maceration/settling time is recorded as part of the manufacturing method description.