What is a Product Information File?
A Product Information File (PIF) is a comprehensive dossier containing all essential data and documentation related to a cosmetic product. It includes detailed information on safety assessments, formulation, and regulatory compliance.
According to the EU Cosmetic Regulation (EC) No 1223/2009, every cosmetic product placed on the European Union (EU) market must have a PIF readily accessible to the competent authorities.
Chemleg’s Product Information File Preparation Service ensures full compliance with EU legislation, allowing you to place your cosmetic products on the market legally and safely.
What should the Product Information File contain?
The PIF must include the following:
- Cosmetic Product Description: Full name, brand, and intended use of the product, along with identifying codes and formulation names that clearly link the product to the file.
- Cosmetic Product Safety Report (CPSR): The CPSR, consisting of Part A and Part B, must be included in the file.
- Manufacturing Method & GMP Compliance: Detailed information on the manufacturing process should be provided. A declaration or certificate confirming Good Manufacturing Practice (GMP) compliance according to ISO 22716 must also be included.
- Evidence of Claimed Effects: Scientific evidence supporting all product claims must be documented in the PIF.
- Animal Testing Data: If applicable, data on animal testing conducted by the manufacturer, its agents, or suppliers for product development or safety assessment must be provided. However, as animal testing on cosmetic products and ingredients is banned in the EU, this section typically includes a statement such as “No animal testing has been conducted.”
- Labeling Information: Label content from both primary and secondary packaging, along with visual examples, must be included.
- Serious Undesirable Effects (SUE): Up-to-date records of any serious undesirable effects reported post-marketing and the measures taken in response must be part of the PIF.
Chemleg’s Product Information File Service
Cosmetic Product Safety Report (CPSR) – Part A & B
- Part A: Ingredient composition, toxicological profiles, exposure assessment
- Part B: Professional safety assessment by a qualified toxicologist
Product Composition & Ingredient Compliance
- Verification of raw materials and compliance with EU ingredient restrictions
- Conformance with the annexes of EC Regulation 1223/2009 (prohibited/restricted substances, preservatives, colorants, UV filters)
Manufacturing & GMP Compliance
- Ensuring compliance with GMP requirements – ISO 22716
- Assessment of product stability and microbiological quality
Labeling & Claims Compliance
- Label review according to EU labeling requirements
- Substantiation of claims based on the EU Commission’s Guidelines on Cosmetic Claims
Cosmetic Product Notification Portal (CPNP) Support
- Assistance with mandatory product notification in the CPNP database
Packaging & Testing Documentation
Why Choose Chemleg’s Product Information File Service?
- Regulatory Expertise: Years of experience in EU cosmetic compliance
- Full-Service Support: From formulation analysis to complete PIF compilation
- Hassle-Free Compliance: Avoid delays, penalties, and market restrictions
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Frequently Asked Questions
What is the difference between PIF and CPSR?
The Product Information File (PIF) is a comprehensive legal document required in both the EU and UK for placing cosmetic products on the market. It demonstrates the product’s safety, quality, and claims. The CPSR is the most critical part of the PIF and serves as formal proof of product safety.
Who is responsible for preparing the PIF?
Legally, the Responsible Person is required to prepare the PIF. According to the EU Cosmetic Regulation, the Responsible Person can be:
- The manufacturer established in the EU,
- The importer placing the product on the EU market,
- An authorized representative appointed by a non-EU manufacturer,
- A brand owner marketing the product under their name.
How long must the PIF be retained?
The PIF must be kept at the Responsible Person’s address for 10 years following the placement of the last batch of the product on the market.
What happens if a PIF is not prepared?
Failure to prepare a PIF may lead to:
- Regulatory penalties and fines
- Market withdrawal or product recall
- Damage to brand reputation
- Customs clearance issues
Should an existing PIF be updated?
Yes. The PIF must be regularly updated. It is a dynamic document that should reflect changes throughout the product’s life cycle.
