REACh

…and I need assistance in the preparation of the technical registration dossier

Equitox

• Searches for and analyses existing data, and submits Inquiries to ECHA,
• Determines the registration strategy,
• Makes exemption requests for product and process-oriented research and development (PPORD),
• Sets out a data acquisition strategy,
• Generates missing data,
• Creates the IUCLID dossier and the Chemical Safety Report (CSR).

…and I would like someone to deal with the administrative part of the registration process for me

Equitox

• Represents you within SIEFs and consortia,
• Ensures compliance with data sharing rules and the cost of the letter of access.
• Manages your REACh-IT account.

…and I would like to update dossiers already registered

Equitox

• Identifies compliance deviations
• Assists with substance identification issues,
• Verifies the strictly controlled conditions (SCC) of intermediates,
• Updates your dossiers with more relevant data to make sure ECHA does not prioritise your substances.

What should I do if my dossier is evaluated?

Equitox

• Explains ECHA’s requests to you,
• Supports you during consultation stages to bring forward admissible arguments likely to challenge the Authorities’ requirements,
• Helps ensure the compliance of your dossier, based on its in-depth knowledge of guidance documents and its technical expertise.

What should I do if my substance is evaluated?

Equitox

• Puts in place an alert on priority substances in your company or on your strategic raw materials, which will be evaluated in the coming years,
• Informs you of issues targeted by the authorities (e.g. PBT, Endocrine Disruptor, etc.) ,
• Helps you answer the questions asked. To do this, Equitox develops all its arguments and expertise to minimise resultant costs.

What should I do in the event of a restriction (project)?

Equitox

• Analyses the impact of this restriction on your markets or raw materials,
• Explores a range of possible options: production shutdown, development of a substitute product, shifts in the production chain, etc.

What should I do if my substance falls under the authorisation process?

Equitox

• Identifies in advance potential future substances of very high concern (SVHC),
• Monitors changes to the candidate list and explains the resulting obligations,
• Informs you of ECHA prioritisation, substances included in annexe XIV and the consequences for your markets,
• Contributes to the preparation of your authorisation dossiers.

I would like assistance in preparing my extended SDSs

Equitox

• Audits your SDSs,
• Drafts annexes to SDSs.

I would like to know whether my use complies with my supplier’s eSDS

Equitox

• Analyses your conditions of use and compares them with those indicated in the exposure scenarios featured in your supplier’s SDS,
• Facilitates exchanges with your suppliers if deviations are identified,
• Outlines possible alternatives in case of non-compliance with the eSDS,
• Draws up the chemical safety report (DU-CSR) taking into account your conditions of use.

I would like assistance in my dealings with national authorities or ECHA

Equitox

• is involved in interactions with the authorities (written communications and meetings),
• Queries help desks in a totally confidential manner,
• Submits notifications to ECHA (authorised use for substance included in Annexe XIV, Candidate list substance in article, use not supported by supplier, different classification).

I would like to be informed of regulatory developments and anticipate future changes

Equitox

• Regularly monitors developments specific to your situation, products and markets,
• Anticipates future regulatory developments (Polymers, PMT),
• Analyses major alerts which may concern your products (classification, restriction, SVHC),
• Analyses regulatory positioning for your R&D projects.

I would like to conduct a Due Diligence review

Equitox

• Audits the product portfolio prior to an acquisition or merger, with a view to clearly mapping out the regulatory status of substances,
• Anticipates possible restrictions or prohibitions which could affect products in the near future.