ISO 22716:2007 Cosmetics — Good Manufacturing Practices (GMP)
ISO 22716:2007 Cosmetics — Good Manufacturing Practices (GMP)
ISO 22716:2007 provides practical guidelines for Good Manufacturing Practices (GMP) in the cosmetics industry. It covers the quality aspects of production, control, storage, and shipment of cosmetic products, helping organizations establish consistent and controlled manufacturing practices.
Implementing ISO 22716:2007 helps cosmetic manufacturers strengthen their quality control, improve operational consistency, support product traceability, and demonstrate their commitment to internationally recognized cosmetic GMP practices.
The standard is designed to support organizations involved in the manufacture and handling of cosmetic products by establishing appropriate controls throughout relevant production and quality processes.
Cosmetic products require consistent manufacturing and quality control to protect product quality and maintain consumer confidence.
ISO 22716:2007 provides a structured framework for Good Manufacturing Practices, covering key operational areas such as personnel, premises, equipment, raw materials and packaging materials, production, quality control, documentation, storage, and shipment.
ISO 22716:2007 focuses on quality aspects and does not cover occupational safety or environmental protection requirements. It also does not apply to research and development activities or the distribution of finished products.
- StandardISO 22716:2007
- CategoryCosmetics GMP
- Edition1st Edition (2007)
- ApplicableCosmetics Industry
- Validity3 Years
- BodyQCert Malaysia
Benefits of ISO 22716:2007
Implementing ISO 22716:2007 standards enhances your organization's capabilities as follows:
Strengthen Product Quality: Establish controlled and consistent processes to support the quality of cosmetic products throughout manufacturing and handling activities.
Improve Manufacturing Control: Create clearer controls for production activities, raw materials, equipment, personnel, premises, and quality-related processes.
Enhance Traceability: Improve the ability to identify and trace materials, production activities, batches, and relevant quality records.
Reduce Operational Risks: Identify and control potential sources of contamination, mix-ups, errors, and other quality-related risks within manufacturing operations.
Improve Documentation: Establish appropriate documented information and records to support consistency, accountability, and effective process control.
Strengthen Customer Confidence: Demonstrate a structured commitment to internationally recognized cosmetic Good Manufacturing Practices.
Support Regulatory & Market Requirements: A robust GMP framework can help organizations respond more effectively to customer, market, and applicable regulatory expectations.
Drive Continual Improvement: Regular review, monitoring, corrective action, and improvement activities can help strengthen the effectiveness of cosmetic manufacturing processes.
How We Do It — GMP Certification Approach
QCert follows a structured certification process to assess the organization's implementation of applicable ISO 22716:2007 requirements.
Plan
Define the certification scope, understand the organization's processes, identify applicable requirements, and prepare the organization for the assessment.
Do
Implement the required procedures, controls, records, and operational practices across relevant cosmetic manufacturing activities.
Check
Evaluate the effectiveness of implemented processes through assessment, review of records, interviews, observations, and verification of controls.
Act
Address identified nonconformities and opportunities for improvement, taking appropriate corrective actions to continually strengthen the system.
Through this structured approach, organizations can establish effective cosmetic GMP controls and demonstrate conformity with the applicable requirements of ISO 22716:2007.
Mandatory Records & Controls
- Scope of Cosmetics GMP Quality Management System
- Personnel hygiene, training, and qualification records
- Premises, sanitation, and equipment maintenance & calibration logs
- Raw material, packaging material, and finished product specifications
- Production batch records, filling logs, and quality control test reports
- Out-of-specification (OOS) handling, deviation logs, and recall procedures
- Internal audit findings, management review records, and corrective action plans
ISO 22716:2007 Certification Cost
The cost of ISO 22716:2007 certification depends on several factors, including the organization's size, number of employees, number of sites, manufacturing activities, process complexity, and certification scope.
At QCert Malaysia, our experienced certification team can help you understand the certification requirements and provide a quotation based on your organization's specific needs.
Grow your business competitiveness in local and international cosmetic markets.
Our experienced lead auditors make your GMP audit process streamlined and hassle-free.
Achieve accredited certification trust and credibility with key stakeholders.
We are just a call away — talk to our team or request a quick quote today.
Sample Certificate & Mark
Preview of the QCert Malaysia issued certification documents. Click any image below to enlarge in Lightbox.
