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The 2018 Quality Assurance Guidelines provide approaches that cosmetic manufacturers can use for establishing their good manufacturing practices and quality assurance programs. The Guidelines provide a framework for establishing systems and procedures that are necessary to achieve a high level of product quality and avoid problems that could adversely affect the product. ISO Standard 22716 is included as a companion reference document with these Guidelines. The new 2018 PDF contains the 2014 information plus a new Annex on Process Verification associated with the production of cosmetic and personal care products.

 

The cost is $525 USD for PCPC members and $1,050 USD for nonmembers. For those who previously purchased a copy of the 2014 version, you can purchase the entire new PDF for the discounted fee of $100 USD for PCPC members and $200 USD for nonmembers. Please note that the purchase of the 2014 Quality Assurance Guidelines PDF Download must be reflected on your individual record in order to get discount pricing. If you have purchased the 2014 version, please login and then select PCPC 2018 Quality Assurance Guidelines (PDF Download) Discount from the main Bookstore page. 

 

Foreword
Acknowledgements
List of Figures
Introduction
ISO 22716 Cosmetics Good Manufacturing Practices
Annex 1 Personnel and Training
Annex 2 Premises (Facility)
Annex 3 Equipment
Part 1 – Packaging
Part 2 – Processing
Annex 4 Raw Materials and Packaging Materials
Annex 5 Production Control
Annex 6 Finished Products/Lot Identification and Control
Annex 7 Quality Control Laboratory Operation
Annex 8 Treatment of Product that is Out of Specification
Annex 9 Recalls
Annex 10 Subcontractor Quality Assurance
Annex 11 Deviations
Annex 12 Consumer Complaints and Comments
Annex 13 Change Control
Annex 14 Internal Audit
Annex 15 Information Management Systems
Annex 16 Calibration Systems
Annex 17 Sampling
Part 1- General Provisions Sampling Plan
Part 2 – Sampling and Control Techniques
Annex 18 Specifications
Annex 19 Indices of Quality Performance
Annex 20 Evaluating New or Revised Products
Annex 21 New Packaging Quality
Annex 22 Classification of Defects
Annex 23 FDA Inspections
Annex 24 Regulatory Compliance Considerations
Annex 25 Process Verification
Appendix PCMAP Checklist
Glossary of Terms