Global management of your regulatory monitoring with EcoWatch
Optimize your regulatory watch with an integrated strategy to anticipate compliance in the short, medium and long term.
Essential
Keep abreast of regulatory developments relevant to your business with a bi-monthly newsletter. Your entire scope is covered, making it easier to understand regulatory changes and meet your obligations with absolute peace of mind.
Newsletter
- Implementation of the monitoring format specific to your needs: summary report by regulation, Excel with a list of substances, color codes to be implemented...etc.
- Adaptation of regulatory content according to the level of expertise expected by the customer.
Regulations : Biocides, Detergents, Cosmetics, Toys, Food Contact, Transport of Dangerous Goods by Road, POPs, PICs, Explosives Precursors, Drug Precursors...
Directives on aerosol cans, worker protection, ROHS WEEE directives, end-of-life vehicles...
Nanomaterials, endocrine disruptors, microplastics, ozone layer and greenhouse gases, AGEC Act, environmentally classified facilities.
- Update of the Newsletter* and feedback meeting with an expert analysis of critical points.
Impact
Assess the regulatory status of your substance portfolio with our Impact offer. We analyze the impact of these regulations on your mixtures, enabling you to make informed decisions for your business.
Screening of your substances
- Analysis of your list of substances and validation of their identity. Identify whether a substance may belong to a regulatory entry of substance families.
- Study of regulatory lists impacting your substances standard European scope (REACH / CLP) : CORAP, PACT, Registers of Intent, CLH, Candidate List, (recommendations) Annex XIV & Annex XVII.
- Screening of your list of substances with the regulatory lists ("matching" of CAS or EC numbers).
- Analysis of obligations and anticipation of regulatory deadlines for each regulatory list impacting one of your substances according to 3 color codes:
- Red - Prohibition: substances belonging to Annex XIV, Annex XVII or "effective" recommendations for inclusion in Annexes XIV or XVII.
- Orange - Alert: substances belonging to the SVHC candidate list or its register of intent.
- Grey - Watch: substances belonging to the PACT, CORAP, CLH lists and CLH register of intent (if CMR hazard category or other REACH art. 56 hazard criteria eligible for the candidate list, then switch to orange).
→ An estimate of regulatory time is also given based on the average time of the history of substances that have been regulated. Monitoring includes the detection of draft texts within the limits of their public accessibility, the follow-up of ECHA activities (registers of intentions, ARN list, etc...), the follow-up of specialized sites....
Fields: Reach, CLP, Toys, POPs, Microplastics, Biocides, Aerosols, PIC; Nanomaterials, Endocrine disruptors, AGEC Act, ICPE, Detergents, Cosmetics, Ozone layers and Greenhouse gases.
Manage your substance portfolio
- Collection of SDS
- Creation of an email box dedicated to receiving customer SDSs, and email campaigns to collect SDSs from your suppliers.
- Sending an SDS by the supplier is preferred. If this doesn't succeed, we'll proceed to upload the SDS onto the websites.
- Extraction of the composition of the SDSs
- Digitization of section 3 of the SDS with the composition of each chemical product.
- Summary of your eligible and relevant substances.
Strategic
Anticipate regulatory developments for your targeted substances with an in-depth impact analysis by an expert. We provide you with the information you need to make strategic decisions for your business.
Prioritization study (advanced substance screening)
- Anticipation of possible prioritization based on substance selection criteria as described in the "SVHC Roadmap to 2020 - Implementation Plan" document (cross-checked with information disseminated on substance classification and use).
- Study of recommendations for inclusion in Annexes XIV and XVII.
- Assessment** of the risk of prioritization of each substance on the 3 aspects :
- The substance's current level of prioritization and the estimated minimum potential time before the substance enters a list.
- The scoring rules linked to the inclusion of a substance in Annex XIV.
- Search for regulatory information on structural analogues for substances without available data and rapid screening of each analogue***.
- Conclusion report on regulatory risks, including:
- Known or possible deadlines (argued) for each substance and an estimated obsolescence schedule based on our regulatory experience and the regulatory cycle of other substances.
- A link to documents, publications... that provide an estimate of this timeframe, enabling you to monitor future developments.
- Actions that the customer should consider as a first analysis.
* According to a defined frequency.
** Depending on the availability of regulatory information, if feasible, a comparison between possible Risk Management Options Analysis (RMOA) options may be conducted.
*** Depending on the availability of regulatory information.
Would you like to optimize your regulatory watch with EcoMundo?
