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The basics

Learn and keep up to date on the essentials of the regulations.

Ancre 1

Biological evaluation of medical devices in accordance with EN ISO 10993-1

from 690€ (HT)

Understand the methodology of biological assessment in accordance with EN ISO 10993-1
Assess the conformity of a biological assessment plan

Familiarise yourself with eSDS: obligations, content and compliance

from 690€ (HT)

Understand the obligations under REACH and the impact/penalties in the event of non-compliance 
Know how to draw up an extended safety data sheet As a downstream user, know how to check your own compliance with supplier SDSs 
Be familiar with the methods for ensuring compliance in the event of discrepancies between downstream uses and the exposure scenarios covered by the eSDS

How do Biocidal Product Families work? Accelerate your time to market!

from 690€ (HT)


Addressing the stages of an application for authorisation of a family of biocidal products : 

- Similarity of composition & grouping of co-formulants 
- Similarity of uses 
- Similar level of risk and efficacy 

Addressing the various points to be taken into account when dividing biocidal product families for current evaluations

Introduction to packaging regulations: understanding and implementing them

from 690€ (HT)

Areas: food contact, cosmetics and pharmaceuticals 


Understand the regulatory prerequisites for cosmetic, food contact and pharmaceutical packaging 
Acquire an overview of the regulatory texts applicable to materials 
Be familiar with the essential requirements and specific features of this legislation 
Understand a container/content risk assessment (LMS)

Master CHESAR to simplify your REACH assessments

from 1035€ (HT)


Understand the obligations under REACH How to use CHESAR to carry out a CSA (Chemical Safety Assessment) 
Be able to generate a CSR (Chemical Safety Report) under CHESAR 
Comply with ECHA expectations

Master IUCLID and register your substances under REACH

from 345€ (HT)


How to navigate and enter data in IUCLID 
Be familiar with the main non-technical sections of a REACH dossier and know how to complete them 
Be able to proofread the technical sections of a REACH dossier 
Know how to use the various features of IUCLID (exports, validation wizards) Be able to submit a dossier in REACH IT

New ISO 10993-17 : 2023 - General and new features

from 690€ (HT)


Understand the methodology for the toxicological assessment of medical device components in accordance with ISO 10993-17:2023.

Regulations in Europe and the USA for recycled plastics
intended for contact with food and in cosmetics

from 148€ (HT)


Be able to describe the basics of European regulation 2022/1616/EC for recycled plastics in contact with foodstuffs 
Be able to describe the basics of US regulations for recycled plastics: No Objection Letters, processes, etc.

Regulatory ecotoxicology: from the appropriate conduct of studies to environmental risk assessment

from 690€ (HT)


Gain a better understanding of why studies are carried out, what the results mean and how they can be used for Classification and Risk Assessment. 
Be able to spot the pitfalls of studies and know how to avoid them

Safer cosmetics for tomorrow - Know your regulatory obligations

from 690€ (HT)


Knowing and understanding Cosmetics Regulation 1223/2009 
Understand the risk assessment of a cosmetic product 
Identify areas for improvement in order to comply with regulatory obligations

Toxicology and Classification - the fundamentals of your regulatory success

from 1380€ (HT)


Understand the role of toxicology in the life of substances in accordance with regulations
Understanding the main tests, their difficulties and the issues involved 
Optimising interaction between managers and experts

What our customers say

"I am very satisfied with this course, which was well adapted to my background and met my needs. Furthermore, the distance learning format is entirely satisfactory, and the limited number of trainees facilitates exchanges."

Certification QUALIOPI - Action de formation

La certification qualité a été délivrée au titre de la catégorie d’action suivante : ACTION DE FORMATION.

About CEHTRA

We have been specialising for 20 years in assisting companies in the marketing of chemical substances or products in France and also in Europe and outside Europe.

 

Our toxicologists, ecotoxicologists and chemists provide you with their expertise to ensure the regulatory compliance of your products.

 

With a team of 70 people, we cover a dozen sectors including REACH, biocides, plant protection products, etc...

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