Slide Did you know that ECA is by far the most effective anti-bacterial agent? Click Here Slide ECA Consortium A/S has in recent years gained extensive experience, and collaborates with leading consulting firms and specialized lawyers Click Here Slide The ECA technology is extremely useful in a wide range of industries Click Here Slide We have the BPR regulation knowledge to help you achieve compliance Click Here

Our services

Product authorization

ECA Consortium A/S generates a core dossier, which will contain everything needed for a product authorization application, including all relevant information for precursor, disinfection liquid, use cases, efficacy test and relevant risk assessment.

The core dossier covers the Biocidal Product Family (8 BPFs) and we have selected the Danish EPA as competent evaluating authority.

ECA Consortium A/S offers their customers to obtain the product authorization in their own name by using information from the core dossier in their Union application.

We offer Letter of Access for product authorization for:

  • In-situ generated active substance – active chlorine generated from sodium chloride by electrolysis:
    Four biocidal families, PT 1, 2, 3, 4, and 5
  • Active substance filled into bottles – active chlorine released from hypochlorous acid:
    Four biocidal families, PT 1, 2, 3, 4, and 5

To ensure that customers comply with the core dossier specifications, customers shall fill out a questionnaire and deliver a 5-batch analysis of the disinfection liquid.

Click Here for more information about BPR on the ECHA Website

Click Here for the latest consolidated version of the BPR legal text, dated 25 April 2014.

Product Authorization UNTIL July 2022

Besides approval of the active substance, the disinfection liquid also shall have a product authorization.

Today (and until July 2022) you must apply for product authorization with the national authorities in the countries where you are selling your products.

Product authorization AFTER July 2022

From 1 July 2022 the product authorization will be handled by the European Union.

For the Union approvals you will be able to buy a Letter of Access for product authorizations from ECA Consortium A/S and make the application in your company name.

The core dossier generated ECA Consortium A/S will contain information necessary for the product authorization application, including information about precursor, disinfection liquid, use cases, efficacy test and relevant risk assessment, what is needed for a product authorization application.

The Core Dossier is built up among Biocidal Product Family (8 BFM) and we have selected the Danish EPA as competent evaluating authority.

ECA Consortium A/S offers their customers to obtain the product authorization in their own name by using information from the core dossier in their Union application.

Our services

Core dossier specifications

The Core Dossier is built up among Biocidal Product Family (8 BFM) and we have selected the Danish EPA as competent evaluating authority.

ECA Consortium A/S offers their customers to obtain the product authorization in their own name by using information from the core dossier in their Union application.

We offer Letter of access for Product Authorization for:

  • In-situ. Active chlorine generated from sodium chloride by electrolysis: 4 biocidal families
  • Bottle: Active chlorine released from Hypochlorous Acid: 4 biocidal families

To secure customers to be inside core dossier specification’s, customers shall fill out an questionnaire, and deliver a 5 batch analyze of the disinfection liquid.

Click Here for more information about BPR on the ECHA Website

Click Here for the latest consolidated version of the BPR legal text, dated 25 April 2014.

Contact

ECA Consortium A/S

Blegen 9 4th, 6400 Sønderborg, Denmark

+45 51 52 61 52

Peter@ecaconsortium.com