ISO 22716 STANDARD PDF

ISO is the standard describing the Cosmetics Good Manufacturing Practices, which are a set of hands-on advice, operational rules and organizational. Reference number. ISO (E). © ISO INTERNATIONAL. STANDARD. ISO. First edition. Corrected version. One way to demonstrate compliance with GMP is to implement the international standard ISO ISO introduces a management systems.

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Read our article to learn more about Good Manufacturing Practices and how to be compliant. This ios deals with GMP for cosmetic products. GMP for pharmaceutical products are different and not covered by this article. Good Manufacturing Practices are practical and organizational guidelines set up to ensure the reproducibility and the quality of the manufacturing process of cosmetic products.

It consists of a couple of measures that have to be implemented in relation to the manufacturing process, control, storage and shipment.

Good Manufacturing Practices (GMP) – ISO 22716 Auditing

Good Manufacturing Practices concern the quality of the cosmetic products. The ISO standard defines the quality and reproducibility of cosmetic products found on the European market.

EcoMundo summarizes here the different points of the ISO standard which describes the different measures to adopt to comply with Good Manufacturing Practices.

This a non-exhaustive list, to get all the necessary information, please refer to the official publication of ISO standard. Therefore it is necessary that the staff have appropriate training, documentation and skills for the manufacture of cosmetics. The purchase of raw materials and packaging for cosmetic items depends on proper selection of suppliers made of specific quality criteria. The next step is to create a dynamic supplier chain of information so as to quickly trace problems that might arise.

The reception and storage purchases depend on strict rules verification, strict nomenclature, accurate labeling, etc. Regarding the water used in production, its quality must be ensured by a system of adequate treatment and testing.

Various measures should be taken during the manufacture of the cosmetic product to obtain a quality product. It is particularly necessary to:. Finished products must meet the quality standards established by the company. Their quality must be maintained during storage operations, shipping and product returns.

Before placing the finished product on the market, it is necessary to verify the compliance with defined quality criteria. Strict rules of storage must be put in place to differentiate the different batches, the returned batches and batches placed in quarantined.

They are made possible by a specific product labeling. The quality control will help to highlight the raw materials, finished products, and packaging items out of specification. The staff in charge of quality control will then treat these nonconformities by measures such as the destruction or recycling of finished products, rejection of raw materials and packaging items. If a deviation to operation of the manufacture is established, this must be noted and justified. The deviation can lead to a decline in quality, a decision must be made for the placing on the market of the finished products.

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The competent staff will then take corrective action so this gap does not happen again.

ISO 22716 cosmetics – good manufacturing practices

The company must define the different types of waste generated by the production process and control of cosmetic products. These must be clearly identified and their disposal must be done in a controlled and sanitary manner: If outsourcing for manufacturing, packaging, testing, cleaning and disinfection of premises, etc.

Just as the choice of supplier, the choice of the subcontractor is done according to specifications. Processes concerning recall operations should allow a fast operation by authorized personnel.

If the 2216 is likely to have an impact on consumer safety, the authorities concerned must be informed and the recalled products should be identified and stored separately pending a decision. In the case of outsourced operations, the contract between the prime contractor and the subcontractor must agree on a process.

Changes affecting the quality of the product must be approved and performed by authorized personnel on adequate database. To ensure the implementation and enforcement of GMP, companies must implement internal audits.

These must be led by the company’s stancard service. The audit team is in charge of setting up and verifying that all guidelines outlined in the ISO standard are correctly implemented. Moreover, standarc case of non-compliance, they are responsible for analyzing deviations in order to find appropriate corrective measures.

Good Manufacturing Practices (GMP) – ISO Auditing

Companies should put in place an updated documentation system to identify activities related to the production, control, storage and shipment of cosmetic products. It can be protocols, instructions, methods, etc. This stancard is verified through an internal audit, or by using a specialized service provider that checks compliance with ISO The ISO certification is necessary for the marketing of cosmetic products.

Although it requires the implementation of strict measures, there is no official certification for this standard. On 10 Julythe European Commission published the list of “common criteria for The Cosmetic Regulation applies to finished cosmetic products, and sets up requirements for By Sabine Ashfaq Expert adviceCosmetics comments. Validate the compliance of business management isso with the requirements of the European Cosmetics Regulation Ensure access to the European market Please note: Which Stakeholders are involved?

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Equipment The equipment used by the company must be designed to: Raw Materials and packaging items The purchase of raw materials and packaging for cosmetic items depends on proper selection of suppliers made of specific quality criteria.

Manufacturing Various measures should be taken during the manufacture of the cosmetic product to obtain a quality product. It is particularly necessary to: Summarize the process of producing the cosmetic product raw materials, formula, and required equipment in an accurate and comprehensive documentation Identify quality control points Number the batch and label them properly for an 227116 identification on the production line Check the cleanliness, safety and calibration of premises and equipment before producing to minimize the risk of product contamination 6.

Finished Products Finished products must meet the quality standards established by the company. Treatment of off-specification and deviations The quality control will help to highlight the raw materials, finished products, and packaging items out of specification. Waste The company must define the different types of waste generated by the production process and control of cosmetic products.

Subcontracting If outsourcing for manufacturing, packaging, testing, cleaning and disinfection of premises, etc. Stamdard and recalls All claims must be investigated with the following elements: The preventive measures against the recurrence of the default The verification of all concerned batches Processes concerning recall operations should allow a fast operation by authorized personnel.

Change Management Changes affecting the quality of the product must be approved and performed by authorized personnel on adequate database. Documentation Companies should put in place an updated documentation system to identify activities related to the production, control, storage and shipment of cosmetic products.

ISO Cosmetics GMP guidelines certification | LR UK

The documentation must be accessible, signed, dated and updated regularly. How to comply with GMP? How to create your cosmetic PIF? Common criteria for cosmetic product claims On 10 Julythe European Commission published the list of “common criteria for Labeling compliance for Europe The Cosmetic Regulation applies to finished cosmetic products, and sets up requirements for Language En ko Fr Standarf comment language code.

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