Introduzione
Global Cosmetic Compliance Made Simple
In an industry where safety, transparency, and speed-to-market are critical, navigating regulatory frameworks is no longer optional — it is a strategic necessity. Professionals working in cosmetics must balance innovation with compliance to ensure that products reach consumers without costly delays, recalls, or reputational risks.
This training offers a comprehensive journey through the EU, US, and Canadian regulations, equipping participants with the knowledge and tools to confidently manage compliance from product development to market launch.
Designed for professionals involved in regulatory affairs, quality assurance, R&D, marketing, and business development, it focuses on the legal and procedural foundations necessary to ensure compliant product development, labelling, safety, and market placement.
The course also emphasizes key differences and similarities between these major markets, with case studies and interactive activities to reinforce practical understanding.
Programme
SESSION 1 – Foundations & the EU Framework
Regulatory Objectives – Global Perspective
- Why cosmetics are regulated
- Key regulatory philosophies: EU vs. US vs. Canada
What is a cosmetic product
- Introduction to Borderline products
- Comparison between EU, US and Canadian definition of a cosmetic product
- Claims correlation to cosmetic definition
EU Cosmetics Regulation (EC) No 1223/2009
- Scope of the regulation
- Horizontal legislation
- PIF & CPSR
Labelling, Claims & Notification
- Mandatory labelling elements (INCI, allergens, PAO, warnings)
- Substantiating cosmetic claims (Regulation 655/2013)
- CPNP notification: overview and workflow
Roles & Responsibilities in the EU
- Economic operators: Manufacturer, Importer, Distributor
- Responsible Person (RP): Legal duties, liability, documentation
SESSION 2 – EU Market Access: From Development to Consumer
From Product Development to Market Entry
- Checklist before placing a cosmetic product in the EU market
- Comparison with Swiss legal framework for cosmetic products
- Product Information File (PIF): Required content and structure
- Cosmetic Product Safety Report (CPSR) examples
- Cosmetics regulation in the UK
US Cosmetic Regulations & MoCRA
- FDA authority under FD&C Act
- MoCRA requirements: facility registration, product listing, safety substantiation, adverse event reporting, GMP
- Key differences vs. EU
Canada’s Cosmetic Regulatory Framework
- Health Canada oversight
- Cosmetic definition vs. borderline products
- Canada´s cosmetic legal framework
- Key differences vs. EU
Comparative Analysis & Final Case Study
- Comparing EU vs. US vs. Canada regulatory ecosystems (notification, GMP, claims, enforcement)
- Case study
- Final Q&A and discussion
- Regulatory Affairs, Registration & Documentation Professionals
- Quality Assurance Officers and Managers
- R&D and Product Development Teams
- Marketing Professionals involved in labelling and claims
- Business Development and Project Management Professionals
- Anyone working with cosmetics intended for the EU, US, or Canadian markets
Participant experience
No prior regulatory knowledge is required.
Delivered as a live online workshop, the training will feature presentations, real-world examples, group discussions, and Q&A.
Docente/i
Claudia Soto
Claudia Soto is a cosmetic chemist and formulator, safety assessor, regulatory consultant, GMP and quality management systems expert and trained COSMOS auditor with extensive expertise in EU and international cosmetic regulations. As co-founder of Seguridad Cosmética, she supports brands worldwide by guiding them from product formulation and development through regulatory compliance and post-market vigilance, ensuring safe, compliant, and successful launches.
Online Training – 2 modules:
MODULE 1 | 10 May 2026 from 2:00 pm to 6:00 pm CEST
MODULE 2 | 12 May 2026 from 2:00 pm to 6:00 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 19/04/2027
Ordinary:€ 990,00*
Freelance – Individual – Academy – Public Administration: € 565,00*
*for Italian companies: +22% VAT
The fee includes: tuition, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Newsletter
Ilaria Butta
Events & Training Manager
Cosa saprai fare dopo il corso
Online interactive training on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before the training.
