Cosmetic Regulatory Affairs | Training LS Academy

Introduzione

Compliance with the regulatory requirements applicable to cosmetic products is crucial to ensure the highest level of safety for consumers.

Placing cosmetic products on the US and Canadian markets involves specific requirements regarding product classification, cosmetic ingredients, labelling and registration.

This introductory course will guide you through the main applicable requirements and provide you with a grounding knowledge of regulatory affairs of cosmetics in the US and Canada.

Overview of US Federal Cosmetics Regulatory Framework

FDA’s authority over Cosmetics
Cosmetic Regulatory Definition
Requirements on Ingredients and Safety Assessment
Labelling Requirements
Animal Testing
Good Manufacturing Practices (GMP)
Voluntary Cosmetic Registration Program (VCRP)
State Cosmetics Regulations
Major regulatory changes for the US Cosmetics Industry in 2023 – MoCRA

Overview of Cosmetics Regulations in Canada

Health Canada’s authority over Cosmetics
Cosmetic Regulatory Definition and Classification
Cosmetic Ingredient Hotlist
Labelling Requirements
Particular Requirements for Certain Cosmetics
Animal Testing
Good Manufacturing Practices (GMP)
Notification of Cosmetic Products

Q&A Session

Professionals in the cosmetic and personal care industries new to US and Canada Cosmetics Regulatory Affairs or wishing to update their knowledge on these regulatory frameworks.
Regulatory Affairs, Registration and Documentation Assistants/Officers/Managers and Quality Assurance professionals seeking to improve their skills in the cosmetic’s regulatory environment.
R&D professionals involved in development of cosmetic formulations for the North America market.
Marketing professionals involved in cosmetics label preparation and market placement.
Project Management or Business Development officers who would find knowledge of the regulatory environment useful.

Training will be in the form of an interactive workshop. It will include presentations, discussions, and Q&A.

Docente/i

Info

Liliana Teles

Quality Assurance & Regulatory Affairs Director – Critical Catalyst

Liliana Teles is a pharmacist holding Masters in Pharmaceutical Sciences and Pharmaceutical Medicine, with more than 10 years of experience in Medical Devices and In Vitro Diagnostics Regulatory Affairs & Quality Assurance. At Critical Catalyst, her work is focused in supporting medical device Manufacturers, Distributors, and Importers in achieving regulatory compliance. Experienced in implementation and audit to Quality Management Systems according to ISO 13485 and Good Distribution Practices of medical devices.
Passionate about working with dedicated teams, driving projects related to regulatory compliance in the medtech field and streamlining patients access to medical device technology.

Durata e Informazioni utili
Quote Iscrizione

Online Training – 2 modules

MODULE 1 | 15 October 2024 from 2.00 pm to 5.30 pm CEST
MODULE 2 | 17 October 2024 from 2.00 pm to 5.30 pm CEST

Some days before the online training you will receive all details about the connection.

The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.

Early Bird: € 790,00* (until 24 September 2024)

Ordinary: € 990,00*

Freelance – Individual – Academy – Public Administration**: € 500,00*

*for Italian companies: +22% VAT

**Early Bird discount not applicable to Freelance – Individual – Academy – Public Administration fee

The fee includes: tuition, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.

Versione Stampabile

Cosa saprai fare dopo il corso

Gain a complete grounding in the fundamentals of the regulatory framework applicable to cosmetic products in the US and Canada markets

Recognize the competent authorities in the cosmetics sector in the US and Canada

Understand the specifics of regulatory cosmetic definition and classification

Understand requirements on cosmetic ingredients and evidence of safety for consumers

Have a solid grasp of the mandatory information to be included in a cosmetic label

Understand the registration requirements for cosmetic products

Online interactive training on Zoom platform.

LS Academy will provide the access link to the virtual platform a few days before the training.

Vedi tutte le edizioni

Fundamentals of Cosmetic Regulatory Affairs

Fundamentals of Cosmetic Regulatory Affairs

The Basics of Regulatory Affairs for Cosmetic Products in US and Canada

Fundamentals of European Cosmetics Regulatory Affairs

The Basics of Regulatory Affairs for Cosmetic Products in US and Canada

Fundamentals of European Cosmetics Regulatory Affairs

The Basics of Regulatory Affairs for Cosmetic Products in US and Canada

Fundamentals of European Cosmetics Regulatory Affairs

Introduzione

Docente/i

Liliana Teles

Cosa saprai fare dopo il corso