Cosmetic Compliance Training
Master FDA & EU Standards for Beauty & Personal Care

The FDA’s Modernization of Cosmetics Regulation Act (MoCRA) enforcement will impact your company. Built by industry and compliance experts, this 8-course library trains you on the new FDA requirements for Facilities Registration, Product Listing, Adverse Events Reporting, Good Manufacturing Practices, and much more.

Develop a complete and accurate understanding of ISO 9001, learn the specific requirements of the standard, recognize the importance and benefits of ISO 9001 Certification, and understand how to achieve and maintain certification.

Learn how to raise, manage, and review deviations, including finding the root cause and the corrective and preventative actions to avoid recurrence.

Learn the essential QA Concepts and Practices required to manage quality in a GMP environment with this cost-saving package of 9 online training courses.  

Learn how to complete essential quality functions in a GMP environment. This training will teach the practitioner how to manage deviations, nonconformances and corrective and preventive actions in GMP environments.

Learn the essential Quality Assurance Concepts required to manage quality in a GMP environment including good documentation practices and management of issues, deviations, nonconformances, and corrective and preventive actions.  

Preservative efficacy testing (PET), also known as the challenge test or preservative test, is crucial for assessing the effectiveness of the preservatives in protecting products from microbial contamination throughout their shelf life.  

Gain an understanding of issue management processes used in a cosmetics Good Manufacturing Practice (GMP) environment.  

This course covers the importance of Good Documentation Practice and the GMP requirements that should be kept in mind while creating and maintaining documentation as well as the GMP requirements for filling and recording information.  

This course covers the types of GMP-related documents required to show compliance in a regulated environment and how to create, maintain, and improve a Document Management System to establish proper document control practices.  

Gain an understanding of deviations in GMP environments, with a focus on root-cause analysis and problem-solving.

Learn the process of dealing with CAPAs in a systematic way in a GMP environment including how to raise, manage and review them.

Learn about Part 11 of Title 21 of the Code of Federal Regulations, which establishes the United States Food and Drug Administration (FDA) regulations for electronic records and electronic signatures.

Learn the requirements of 21 CFR 58 (Good Laboratory Practices for Nonclinical Studies), providing additional context and study examples to enhance your understanding of key concepts and of GLP applicability to cosmetics labs.  

This course will focus on dealing with non-conformances systematically in a GMP environment.  

Gain an understanding of the handling of nonconformances in a GMP environment.

This training provides you with an introduction to corrective and preventative actions (CAPA) and how they are used.