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 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
Novel Food & Toxicological assessment: Selecting, understanding and interpreting key studies
from 690€ (HT)
Understand the role of toxicological studies in Novel Food dossiers.
Identify the types of relevant studies depending on the nature of the product.
Read and interpret key data from study reports.
Identify quality and compliance criteria (OECD, GLP).
Efficiently manage and communicate with subcontracted laboratories.
