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ISO Standard Cert
HOME > ISO Standard Cert > ISO 22716 Cosmetics
ISO 22716 Cosmetics
ISO 22716 (Cosmetics – Good Manufacturing Practices(GMP) – Guideline on Good Manufacturing Practices) Overview
ISO 22716 is a guideline for the excellent manufacturing management standards (GMP) of the cosmetics manufacturing industry and describes the requirements for GMPs to be applied by companies that produce cosmetics. ISO 22716 consists of a total of 17 requirements, based on infrastructure management such as human resources, buildings, equipment, etc., manufacturing management from raw materials to finished products, process management from departure/breakaway/discontent and post-processing, and system management, internal review and documentation management. These requirements ensure reliability in cosmetic safety manufacturing from customers by complying with legal requirements while also complying with common requirements from the international community.
ISO 22716 (Cosmetics – Good Manufacturing Practices(GMP) – Guideline on Good Manufacturing Practices) Feature and backgrounds
Currently, most of the components used in the manufacturing and production processes are thoroughly inspected and evaluated. ISO 22716 not only provides guidelines for business plans, but also shows willingness and efforts to ensure the safety, quality and excellence of products.
Companies are screened and inspected in the following areas of the production process in accordance with the ISO 22716 standard.
Companies are screened and inspected in the following areas of the production process in accordance with the ISO 22716 standard.
ISO 22716 (Cosmetics – Good Manufacturing Practices(GMP) – Guideline on Good Manufacturing Practices) Contents
No. | Title |
---|---|
3 | Personnel |
3.1 Principle 3.2 Organization 3.3 Key responsibilities 3.4 Training 3.5 Personnel hygiene and health 3.6 Visitors and untrained personnel |
|
4 | Premises |
4.1 Principle 4.2 Types of area 4.3 Space 4.4 Flow 4.5 Floors, walls, ceilings, windows 4.6 Washing and toilet facilities 4.7 Lighting 4.8 Ventilation 4.9 Pipework, drains and ducts 4.10 Cleaning and sanitization 4.11 Maintenance 4.12 Consumables 4.13 Pest control |
|
5 | Equipment |
5.1 Principle 5.2 Equipment design 5.3 Installation 5.4 Calibration 5.5 Cleaning and sanitization 5.6 Maintenance 5.7 Consumables 5.8 Authorizations 5.9 Back-up systems |
|
6 | Raw materials and packaging materials |
6.1 Principle 6.1 Principle 6.3 Receipt 6.4 Identification and status 6.5 Release 6.6 Storage 6.7 Re-evaluation |
|
7 | Production |
7.1 Principle 7.2 Manufacturing operations 7.3 Packaging operations |
|
8 | Finished products |
8.1 Principle 8.2 Release 8.3 Storage 8.4 Shipment 8.5 Returns |
|
9 | Quality control laboratory |
9.1 Principle 9.2 Test methods 9.3 Acceptance criteria 9.4 Results 9.5 Out-of-specification results 9.6 Reagents, solutions, reference standards, culture media 9.7 Sampling 9.8 Retain sample |
|
10 | Treatment of product that is out of specification |
10.1 Rejected finished products, bulk products, raw materials and packaging materials 10.2 Reprocessed finished products and bulk products |
|
11 | Wastes |
11.1 Principle 11.2 Types of waste 11.3 Flow 11.4 Containers 11.5 Disposal |
|
12 | Subcontracting |
12.1 Principle 12.2 Types of subcontracting 12.3 Contract giver 12.4 Contract acceptor 12.5 Contract |
|
13 | Deviations |
13.1 Deviations from the specified requirements should be authorized with sufficient data to support the decision. 13.2 Corrective action should be made to prevent recurrence of the deviation. |
|
14 | Complaints and recalls |
14.1 Principle 14.2 Product complaints 14.3 Product recalls |
|
15 | Change control |
Changes that could affect the quality of product should be approved and performed by authorized personnel on the basis of sufficient data. | |
16 | Internal audit |
16.1 Principle 16.2 Approach 16.3 Follow-up |
|
17 | Documentation |
17.1 Principle 17.2 Type of document 17.3 Writing, approval and distribution 17.4 Revision 17.5 Archiving |
ISO 22716 (Cosmetics – Good Manufacturing Practices(GMP) – Guideline on Good Manufacturing Practices) Introduction Effectiveness and Necessity
- 1) Prevent and minimize product accidents.
2) Improving the effectiveness and suitability of factory GMP execution.
3) Continuous improvement and risk management related to cosmetics.
4) Responding to customer inquiries due to diversification of products and services.
5) Quality and safety compliance management within the supply chain.
6) Exemption from evaluation during GMP audit of some overseas cosmetics (e.g., GMP in Iran)
7) High evaluation when evaluating visits to overseas customers.
8) Reinforcement of export competitiveness of cosmetics products by proving international quality competitiveness.
The U.S Certification Body is constantly striving to become a company of customer satisfaction by securing sincere and experienced judges so that domestic and foreign companies can implement the introduction of ISO 22716, which is internationally recognized. In addition, I am confident that I can overcome various crises that domestic and foreign companies may face in the future by establishing and implementing an internationally recognized quality system.