Consultare privind substanțele susceptibile de înlocuire
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Consultări
- Consultări în procesul de autorizare
- Identificarea substanţelor care prezintă motive de îngrijorare deosebită
- Proiect de recomandare pentru includerea în lista de autorizare și consultare
- Cereri de autorizare
- Restricții prezentate în curs de examinare
- Cereri de observații și doveziCereri de observații și dovezi
- Propuneri de testare
- Consultări privind clasificarea și etichetarea armonizată
- Consultări specifice privind clasificarea și etichetarea armonizată
- Consultare la solicitarea directorului executiv al ECHA
- Consultare privind substanțele susceptibile de înlocuire
- Consultare privind derogarea de la criteriile de excludere
- Previous consultations on ECHA’s Executive Director Requests to the Committees
- Consultări ca urmare a solicitărilor adresate comitetelor de către directorul executiv al ECHA
- Consultare pe marginea proiectului de recomandare privind modificarea listei de substanțe care fac obiectul autorizării
- Occupational exposure limits - Call for comments and evidence
- Occupational exposure limits – Consultations on OEL recommendation
- Derogations for the protection of cultural heritage
- Proposals for new POPs
- Other calls for comments and evidence
- Consultation on draft recommendation for inclusion in the Authorisation List
Consultare privind substanțele susceptibile de înlocuire
Consultare privind substanțele susceptibile de înlocuire
If an active substance meets any of the criteria for substitution listed in Article 10(1) of the Biocidal Products Regulation (BPR), then the evaluating competent authority may identify the substances as a potential candidate for substitution.
If this is the case, before submitting its opinion on the approval or renewal of the active substance to the Commission, ECHA will launch a consultation on the active substance in question.
During the consultation the following information is made public:
- substance identity (name and EC/CAS numbers)
- product-type(s),
- evaluating competent authority,
- intended uses
- condition(s) of Article 10(1) that are met
This applies to applications for approval or for renewal of approval of active substances, including review programme substances
Consultation process
The consultation gathers relevant information on the availability of substitutes or alternatives to the active substance in question. Information on the availability of possible alternatives is highly important to support the comparative assessment that is required for the authorisation of biocidal products containing the active substance (considered as a candidate for substitution).
The consultation lasts for 60 days.
Interested third parties may submit relevant information using a secure web-form.
The information submitted may be non-confidential or confidential. If you claim information to be confidential, you will need to provide a justification. Any information claimed confidential will only be available to members of the Biocidal Products Committee (BPC), the Member State competent authorities and the BPC Secretariat in ECHA.
All non-confidential information submitted during the process will be made available to the BPC members, accredited stakeholders and applicant(s) for the active substance. The non-confidential comments will also be available on the dedicated pages of the ECHA website.
At the end of the consultation period, the Biocidal Products Committee (BPC) will take into account the confidential and non-confidential information received before finalising its opinion.