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Home / How Can I Access the Products Uploaded to Cpnp ?

How Can I Access the Products Uploaded to Cpnp ?

How it works

Cosmedesk automates the PIF generation as required by Eu regulation

Create/Add together Ingredients

The Regulation lays down rules for ingredients selection, substances authorized, restricted and prohibited for use in cosmetics.

To ensure the safety of a cosmetic production, toxicological data on its ingredients must be completed, for all relevant toxicological endpoints, in order to summate the Margin of Safety (MoS) and perform the prophylactic cess of the cosmetic product.

With Cosmedesk, you tin create and manage your own cosmetic ingredients or we can provide you their toxicological assay upon asking.

Create/Add Raw Materials

Insert the data on the microbial and physico-chemic specifications, impurities and composition of the raw fabric, including data on the presence of allergens to guarantee quality command and product safety.

Upload your raw materials technical documents such as the Safe Data Sail (SDS), the Technical File (TF), The International Fragrance Association (IFRA) certificate, etc., as provided by manufacturers to ensure traceability.

Store, manage and reuse all your raw materials´ data.

Create/Duplicate Products

  • Products Formulation

Throughout the life of a corrective product, some points need to be taken into account, including the careful ingredients and raw materials selection, adequate packaging and appropriate labelling.

Cosmedesk allows y'all non only to create and duplicate your products merely likewise to manage them, from their conception to the estimate of the exposure levels.

  • Label Review

The Regulation deliberates a set of strict requirements for labelling of cosmetic products and o ne of the legal obligations to guarantee consumer safety, is to ensure compliance with these rules. Without proper labelling, a production volition not be immune into the European market.

Cosmedesk allows you to upload your cosmetic production label and artwork and provides a checklist to help yous make sure that it is compliant with the Regulation.

  • Rubber Evaluation

In lodge to demonstrate the safety of a cosmetic production, a comprehensive safety evaluation must be completed.

A typical safety evaluation comprises the post-obit steps:

  1. Take chances identification: based on the toxicological contour and the physical and chemical properties of the ingredients.
  2. Exposure Assessment: based on the declared functions and uses of a substance as corrective ingredient, the corporeality present in the respective cosmetic production categories and their frequency of use.
  3. Dose-response assessment: determination of a Betoken of Departure (POD) normally a No Observed Adverse Effect Level (NOAEL), to establish the relationship between the exposure and the toxic response.
  4. Take chances characterization: adding of the Margin of Safety (MoS), which is the ratio between a PODsystemic and an judge of the exposure, represented by a Systemic Exposure Dose (SED).

Cosmedesk automatically calculates the SED and the MoS for each corrective ingredient, according to SCCS Notes of Guidance for the Testing of Cosmetic Ingredients and their Safety Evaluation (11thursdayRevision).

Generate Documents

  • PIF

The Product Information File (PIF) is the mandatory compilation information of the technical documentation required for every cosmetic production to be placed on the Eu market place. The PIF should exist kept for 10 years later the last batch is placed on the market place and shall include the following information:

  1. Description of the cosmetic product
  2. Cosmetic Product Safety Report (CPSR)
  3. Manufacturing method
  4. Proof of the alleged furnishings
  5. Data on animal testing
  • CPSR

The Cosmetic Product Safety Report (CPSR) is the most important part of the PIF and ensures that a safe assessment has been conducted. According to the Regulation, the CPSR shall contain the following information, organized in two sections:

    1. Production's proper noun and description
    2. Qualitative and quantitative limerick of the product
    3. Physical and chemical characteristics and stability of the cosmetic product
    4. Microbiological quality
    5. Impurities, traces, data about the packaging material
    6. Normal and reasonably foreseeable utilize
    7. Exposure to the cosmetic product
    8. Exposure to the ingredient
    9. Toxicological profile of the substances
    10. Undesirable effects and serious undesirable effects
    11. Information on the corrective product
    1. Assessment conclusion
    2. Labelled warnings and instructions of employ
    3. Reasoning
    4. Assessor'south credentials and approving of role B
    5. Bibliography
  • Labelling Compliance

Cosmedesk provides a checklist with the characterization requirements to ensure labelling compliance and organizes the listing of ingredients in descending guild of their weight at the time they are added to the cosmetic product, also taking into account the allergen restrictions.

  • PaO Interpretation

The Period later Opening (PaO) represents the menstruation of time subsequently opening for which the product is safe and can exist used without any harm to the consumer. Cosmedesk can provide an additional document with the PaO estimation according to the guidelines "Recommandations relatives a l'interpretation de la periode apres ouverture" from the Agence française de sécurité sanataire des produits de santé (ANSM) .

  • Technical Information Sail

Cosmedesk automatically generates the Technical Information Sail, an additional certificate with an overview of your products more than relevant information.

  • CPNP Data Sheet

Cosmedesk offers a certificate with necessary information regarding the formulation to upload during the registration of the product in the Cosmetic Product Notification Portal (CPNP).

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Source: https://www.cosmedesk.com/how-it-works/