Biocides

Chemicals (REACH)

Cosmetics

Pharmaceuticals

Plant Protection

Our project « Chèque transformation Numérique » has received a grant from the European Union under the FEDER-FSE Aquitaine 2014-2020 operational program.

CEHTRA is contributing to the on-going efforts in fighting COVID-19.

CEHTRA is contributing to the on-going efforts in fighting COVID-19.

To help ensuring a rapid availability of disinfectants across the EU during COVID-19 pandemic, a Practical Guide on Fast-Tracking the Supply of Disinfectants has recently been published with the initiative of AISE International Association for Soaps, Detergents and Maintenance Products, EBPF (the European Biocidal Products Forum) and FECC (the European Association of Chemical Distributors) with voluntary contributions from Fieldfisher Belgium, Steptoe & Johnson LLP and CEHTRA. The version 1.2 of this guide was made available on the 27th April. Got questions? Our Biocides expert Nathalie Hanon will be happy to provide more details.

IUCLID dossier will be soon required for all new active substance applications

In the framework of the implementation of the EC General Food Law and the Transparency Regulation, a IUCLID dossier will have to be submitted for every new active substance application from March 27th, 2021, and later in 2021 for renewal submissions. However, the CADDY dossier may not be immediately withdrawn and could still be required by some Member States. Therefore, applicants may be compelled to submit both IUCLID and CADDY dossiers.

CEHTRA has a long experience with both software systems: CADDY for the PPP regulation and IUCLID for REACh and Biocides regulations. Moreover, we can help you for the whole registration process, from data gap analysis to the final dossier submission and beyond, including IUCLID and CADDY dossiers.

ANSES' deadline for Co-formulants

COMMISSION REGULATION (EU) 2021/383 amending Annex III to Regulation (EC) No 1107/2009 entered into force on 24 March 2021.

This Annex III lists the co-formulants which are unacceptable because of their toxicological profile, PBT/vPvB or endocrine disrupting properties.

To comply with regulatory timeline for amendment or withdrawal of the authorisations of Plant Protection Products and adjuvants containing these unacceptable co-formulants at national level, French National Competent Authorities require that complete information on all Plant Protection Products, adjuvants and mixt products that are authorised in France must be provided to ANSES’ services
before 31 May 2021.

Need some support to meet this short timeline?
Our Plant Protection experts Philippe ADRIAN, Estelle BELTRAN and Blandine JOURNEL can help you!

Introducing a new CEHTRA Service: Poison Centre Notifications (PCN)

CEHTRA is pleased to announce the launch of a new service for Poison Centre Notification (PCN).
As an Importer or a downstream user placing hazardous mixtures (with a health and/or physical effect classification) on the EU market you need to provide specific information on their mixtures to centralized EU poison centre before placing their mixture on the market. CEHTRA can support as a third party representative to assist in these requirements.

Our key PCN services:
1) Portfolio Review - Screen your Portfolio to identify mixtures that require PCN and notification deadlines
2) Review Safety data sheets and labels - Full compliance review of SDS and labels
3) Prepare and submit PCN notification - Screen for full notification information and generate UFI codes
4) Regulatory support -Offer regulatory advice on how best to fulfill obligations
Visit our dedicated page for PCN services for more information: https://www.cehtra.com/pcn