The need to update PIF and CPNP files is not limited to commercial changes initiated by your brand. It also includes legal and regulatory changes introduced by European authorities, such as updated restrictions concerning fragrance allergens.
Failing to account for these regulatory requirements, or manufacturing new batches using outdated formulations, may result in products being restricted, withdrawn, or removed from the market. To help your business maintain regulatory continuity without unnecessary disruption, Jasmine explains the periodic review process and the regulatory coordination required between the parties involved in production. This guide covers:
- Steps to establish the reference version of the perfume Product Information File (PIF)
- Assessing the impact of commercial changes on the CPSR and product packaging
- Procedures for adding new fragrances or sizes and managing them through the CPNP
- Adapting to updates in EU regulations and fragrance allergen requirements
- How Jasmine implements private label perfume changes, along with common questions about PIF and CPSR files
Steps to establish the reference version and document the perfume product information file (PIF)
Before making any change to an existing product, you need a single reference point that represents the version currently approved and actually placed on the market. This reference version should be documented through a clear set of data that allows every future modification to be accurately compared against it:
- Approved product name and Stock Keeping Unit (SKU)
- Fragrance code or the perfume’s chemical formulation
- Formulation version and fragrance oil concentration
- Approved product volume and net content
- Packaging version and approved outer packaging structure
- Specifications of the bottle, spray pump, and cap used for the product
- Approved printed artwork version
- Approved ingredient list using INCI nomenclature
- Marketing claims used to promote the product
- Current Cosmetic Product Safety Report (CPSR) version
- Notification status and reference number registered through the CPNP
- Date on which the version was approved and officially became effective
- Batch number of the first production run manufactured under that version
Keeping the product name unchanged is not enough. The ingredients, volume, packaging components, or artwork may all change while the commercial name remains the same. For this reason, each version should be assigned a clear sequential version number rather than vague labels such as “final” or “new.”
The Product Information File (PIF) should also be kept up to date whenever relevant changes occur and retained by the Responsible Person in Europe for ten years after the date on which the last batch of the cosmetic product was placed on the market.
When managing an existing product, the approved reference version becomes the baseline against which all future changes are assessed. At Jasmine, we link the approved formulation, packaging, and artwork to the specific version released for production, making it easier to identify and control any modifications when a repeat order is placed. Contact us today to confirm that your product files are ready for the next production cycle.
Read also: Perfume Product Specification Sheet: 7 Details That Protect Your Project Before Production

How to determine the impact of commercial changes on the CPSR
Not every product change affects its regulatory documentation in the same way. Some changes may require a reassessment of product safety, while others may affect only packaging information or notification data. Determining the correct regulatory action therefore begins with identifying exactly what has changed.
Formulation changes that may affect the CPSR
These may include:
- Changing the fragrance compound used in the approved formulation
- Replacing raw materials or changing their technical specifications
- Approving a new supplier whose technical data differs from the existing one
- Changing the percentage of fragrance concentrate
- Changing the proportion of alcohol or other solvents
- Adjusting the concentration to create a new product formulation
- Changes to the ingredient or allergen list
- New safety information becoming available for any of the ingredients
In these cases, the revised version should be compared with the currently approved version. The Responsible Person and Safety Assessor then determine whether the change requires a new or updated safety assessment. If the change affects information already submitted through the CPNP (Cosmetic Products Notification Portal), the notification data may also need to be reviewed or updated.
Packaging changes and the perfume compliance file
The formulation may remain unchanged while the information presented to consumers is modified. For this reason, it is important to distinguish between changes to the label or printed artwork and changes to the packaging itself.
When modifying a label or printed design, first determine whether the change affects:
- Product name
- INCI ingredient list
- Responsible Person details
- Warnings and directions for use
- Nominal content
- Required language
- Marketing claims
- Any other mandatory regulatory information
A purely visual design change does not automatically require an update to the Cosmetic Product Safety Report (CPSR). However, if legally required information changes, the version retained in the Product Information File (PIF) and, where applicable, the information submitted through the CPNP should be updated.
Any new or revised marketing claim should also be supported by appropriate evidence.
The situation is different when a packaging component that directly contacts the formulation, or that may affect product preservation and use, is changed. Examples include:
- Bottle
- Spray pump or dispenser
- Gasket
- Closure system
- Any material in direct contact with the formulation
- Overall product capacity
In such cases, the compatibility of the new packaging with the perfume may need to be assessed before it is approved for production.
Adding new fragrances and sizes through the CPNP
The required action depends on how significantly the new version differs from the existing product. Common scenarios include:
- Launching the same formulation in a different size
- Using new packaging for the same formulation
- Introducing a new fragrance to the range
- Changing the concentration of an existing fragrance
- Combining existing products into a gift set
- Creating a new SKU based on an existing formulation
Updating product information file documentation
The scope of the update is determined by assessing how the change affects the product identity, formulation, safety assessment, label, packaging, CPNP information, and marketing claims.
If a change does not affect product safety, it may be sufficient to document the new version and update only the relevant section of the Product Information File (PIF). More substantial changes involving the formulation or product safety may require broader regulatory action, as determined by the Safety Assessor and Responsible Person.
The following table provides an initial overview of how some of the most common changes to private label perfume requirements in Europe may affect the regulatory files and the manufacturer’s responsibilities:
| Type of Change | Product Information File (PIF) | Safety Report (CPSR) | CPNP Notification | What the Manufacturer Provides |
| Formulation change | Update affected information | Assess the impact of the change | Review the change and notification requirements | Provide the new formulation |
| Concentration change | Update where required | Safety assessment | Review and update applicable data | Confirm the new concentration |
| Label change | Update the retained version | Depends on the nature of the change | When notification data changes | Provide the approved artwork |
| Packaging change | Update packaging information | Depends on the impact of the packaging material | Depends on the affected data | Provide technical packaging specifications |
| Adding a new size | Document or update the version | Depends on the effect on exposure | Review applicable data | Provide the new SKU and size |
| Adding a new fragrance | Create and document the new version | Conduct a safety assessment | Take the appropriate notification action | Provide the new formulation and SKU |
| New marketing claim | Update supporting evidence | Depending on any safety implications | Depending on the affected data | Provide the approved claim wording |
Whenever you submit a new modification to Jasmine, we record the changes made to the formulation, packaging, or printed artwork and link them to the version approved for production. The relevant compliance party then determines how these changes affect the PIF, CPSR, and CPNP before the revised version is approved.
Read also: When Should You Update a Perfume Product Information File (PIF)?
CPNP requirements when adding new fragrances and sizes
Any requested modification should be converted into a formally approved product version before manufacturing the new batch begins. This prevents production from proceeding according to specifications that no longer match the legally approved version. The process should therefore include:
- Open a change request: Record the current version, the requested modification, the reason for the change, and the affected SKUs.
- Assess the impact of the change: Determine whether the formulation, PIF, CPSR, or CPNP notification is affected.
- Conduct a safety assessment: Refer any safety-relevant changes to the qualified Safety Assessor before approval.
- Update affected files: Revise the documents and regulatory records affected by the change according to the assessment findings.
- Approve packaging and artwork: Finalize the required regulatory information before approving the final print-ready artwork.
- Create a new version: Assign the revised product a clear and traceable version number or approved revision code.
- Release the version for production: Link the approved version to the relevant SKU and manufacturing order.
Approving a new version does not mean deleting the previous one. A complete change history should be retained so that every revision can be traced, using a record such as the following:
| Date | Stock Keeping Unit (SKU) | Previous Version | Requested Change | New Version | Regulatory Status |
| — | — | — | — | — | — |
This record ensures that each production batch can be accurately linked to the formulation, packaging, and printed artwork used for that specific version.
Assigning approved version codes to manufacturing orders helps prevent any batch from being produced according to outdated or non-compliant specifications. To update shipment information and maintain accurate regulatory records, consult our specialist team to review the applicable update requirements.

How to assess the impact of EU regulatory updates on perfume files
Your product may remain commercially unchanged while the CPNP notification requirements that apply to it are updated. The existing product version should therefore be reviewed whenever any of the following changes occur:
- Updated safety data for a raw material or the availability of new technical information
- New specifications issued by a supplier that change the sourcing requirements for specific ingredients
- Changes to the technical information of the fragrance compound or updates to the fragrance concentrate specifications
- New restrictions or bans affecting the use of a chemical substance or its permitted concentration
- Amendments to one of the annexes of the EU Cosmetics Regulation
- Changes to fragrance allergen requirements or disclosure thresholds
- Updates to INCI information or standardized cosmetic ingredient names
- New information concerning undesirable effects or potential risks
- Changes to labelling requirements or mandatory packaging information
- New technical information requiring marketing claims to be reassessed
When any of these changes occurs, the review process should include:
- Identifying the substance or regulatory requirement that has changed
- Identifying all affected products and SKUs
- Comparing the new information with the currently approved formulation, label, and regulatory files
- Referring the impact to the Responsible Person and Safety Assessor whenever product safety or the safety assessment may be affected
- Updating the PIF, CPSR, CPNP information, or label according to the assessment findings, without unnecessarily modifying unaffected files
- Approving the revised version before it is used for any subsequent production batch
When new regulations are introduced or updated safety information becomes available, the relevant compliance party reviews how the change affects your product and its regulatory documentation, including the label and supporting files. At Jasmine, once the revised version has been approved, we implement the required changes to the formulation, packaging, or artwork specifications and link them to the version scheduled for production.
Read also: Perfume Manufacturing Quality Control Before Production
How does Jasmine implement private label perfume changes before reproduction?
At Jasmine Factory in Turkey, once the required approvals have been completed on your side, we convert the approved changes into clear manufacturing instructions that can be implemented directly in the new order. Each revised element is accurately matched to the product version entering production. This includes the following procedures:
- Confirming the approved modifications and incorporating them into the manufacturing specifications for your order
- Matching packaging components and printed artwork to ensure they correspond to the approved product version
- Verifying materials and production preparations to ensure that all components comply with the revised specifications
- Removing conflicting instructions and discontinuing the use of superseded files or cancelled production directions
- Reviewing the production order against the final approved specifications before manufacturing begins
Assessing how a change affects the Product Information File (PIF), CPSR, or CPNP notification remains the responsibility of the regulatory party responsible for your product. Jasmine’s role is to ensure that the approved version is implemented correctly and accurately during manufacturing.
To begin implementing the approved changes for your next order, request the updated formulation information from our factory.

FAQs about perfume product information file
Does every change to a perfume formulation require a new CPSR?
No. The impact of the change should first be assessed. The Safety Assessor then determines whether the existing CPSR needs to be updated or whether a new safety assessment is required.
Does changing a raw material supplier automatically require the product file to be updated?
Not necessarily. What matters is whether the raw material specification, safety data, or any information used in the original product assessment has changed.
Can previous versions be deleted once a new version is approved?
It is generally better to retain them. Keeping previous versions allows you to identify which version was used for each production batch and link it to the regulatory documents that were valid at the time of manufacture.
Is It enough to treat the product as the same product if only the packaging size changes?
Not necessarily. The decision cannot be based on size alone. The product configuration, packaging, and information associated with the relevant version should all be reviewed before determining which regulatory files or records need to be updated.