An Introduction to ISO 22716 - GMP (Good Manufacturing Practice) for Cosmetic Products Training Course

Overview

Compliance with the international guidelines, standards and directives applicable to the production of cosmetics is essential for commercial success and consumer safety. As in the pharmaceutical, medical device and food industries, cosmetic products and their production are constantly inspected to ensure they consistently meet certain standards.

The ISO 22716 standard is a combination of rules that combine ISO 9001 and GMP guidelines.  A cosmetic manufacturer that has the ISO 22716 standard is obliged to strictly comply with a wide variety of rules, from the selection of raw materials to the number of particles that must be present in the production environment, from the microbiological tests to the quality of the water used, from the qualifications of the personnel it employs to the production records it keeps.

This course has been designed to provide an essential overview of GMP in the production and manufacture of cosmetics. It will be particularly useful for Pharmaceutical and Biotech companies/personnel considering entering this market and it will also provide an opportunity for those who need to refresh their knowledge about the requirements.

The programme will cover all aspects of the ISO 22716 standard and will include practical application examples.  The critical points to be considered in the cosmetic production process will be addressed and there will be plenty of time to discuss the complexities involved.

This course is part of our GxP (Good x Practice) training course collection, which feature a variety of topic areas to ensure you comply with the regulations and quality guidelines.

Benefits of Attending

• Understand how to comply with International Cosmetics Directives and Legislation
• Refresh your knowledge about the current Cosmetics GMP requirements
• Know how to establish an ISO 22716 compliant Cosmetics Quality Management System
• Learn how to qualify manufacturing areas: water, HVAC, Gas systems
• Know how to calibrate, clean, maintain, and qualify a system and equipment
• Understand how to validate processes, cleaning, and computerised systems
• Know how to handle an Out of Specification (OOS), an Out of Trend (OOT), deviations, and unexpected incidents
• Hear how to launch a root cause analysis, and prevent human errors
• Gain a better understanding of which elements can trigger a change control initiative

Who Should Attend

Personnel from the following departments:

• Quality Assurance and Quality Control
• Validation
• R & D
• Audit
• Regulatory
• IT
• Warehouse and supply chain
• Engineering
• Procurement

Enrol or reserve