EU Cosmetic Compliance Requirements

The requirements to achieve EU cosmetic compliance can seem close to impossible when you first hear of them, but they’re not. It is actually a straightforward process of document collection to comply with EU cosmetic regulations once you know what you are looking for.

This series of workshops take you through the documents required by EU regulators and explains how to meet compliance requirements without the usual headaches.

Start Date: Can be started at any time.

Duration: 1 month lecture access.

Assessment: None.

Course Type: On-Line Workshops. Note: Workshop is self-training, so won’t include trainers support if you have further questions.

Study this workshop with us and get the cost of these workshops back if you enrol in our Certificate in Cosmetic Regulatory Essentials later!

Pay with EURO

Price:295€ for set of 4 lectures and text.

NOTE: For immediate access once purchased, stay on PayPal page for access details

PAY WITH AUD

Price: $495AUD for set of 4 lectures and text.

NOTE: For immediate access once purchased, stay on PayPal page for access details

Contents:

Detailed text to accompany the lectures
Worked examples to follow the learning and help you put the learning into practice immediately
1-month unrestricted online workshop access (4 lectures)

You will learn:

Workshop 1: Understanding and searching EU Regulations

How EU regulates cosmetic products
How to conduct searches of EU regulations
How to conduct searches of EU cosmetic ingredients, limits, restrictions and prohibitions
How to check compliance of preservatives, sunscreens, colours, active ingredients, purity, nano-materials and allergens

How to check composition of ingredients

Workshop 2: Labels and claims

A detailed explanation with examples of how to properly prepare ingredient lists
How to prepare labels with all required label information
All required label information, and how it must be presented
How to determine suitable claims and evidence to support claims

EU Free From rules and how to comply

Workshop 3: Responsible Person and the Product Information File (PIF)

Who can be your Responsible Person
Duties of the Responsible Person
How to prepare your Product Information File (PIF)
What information is essential in your PIF
Testing required: stability, preservative efficacy, performance evaluations
What documents and evidence is required with your PIF
PIF template and worked examples provided

Workshop 4: The safety assessment and evaluation

What is required in a safety evaluation and who can conduct it
How to perform safety calculations and the safety assessment
Required safety summaries and statements
Documents required to support the safety assessment

These workshops are ideal for:

Those wanting to understand EU compliance requirements
Marketing and/or regulatory staff involved with label preparation
Regulatory and/or R&D staff involved in preparing their own PIFs
Regulatory, R&D and/or consultants wanting to prepare documentation for/to conduct safety evaluations