OUR SERVICES
We help companies navigate EU biocide regulation and achieve compliance with Article 95 and product authorisation requirements.
Whether you are an end user, manufacturer, or distributor, we offer tailored regulatory support.
Services we offer
Article 95 Listing Support
We guide you through achieving Article 95 status for active chlorine — whether generated in-situ or as a filled product.
Product Authorization Support
Support in preparing and submitting product authorisation dossiers at national or Union level.
Core Dossier Access
Access to our core dossier containing product specs, use cases, efficacy data and more.
By-product Letters of Access (LoA)
We offer support and documentation for LoAs relating to biocidal by-products.
Regulatory Guidance & Documentation
Assistance completing questionnaires, submitting batch analyses and engaging with authorities.
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Who we help
We support a range of customers working with active chlorine and ECA technology — from direct users to manufacturers and distributors.
End Customers
Confirms compliance when using active chlorine directly.
Liquid Manufacturers / Distributors
Compliance paths for bottled, marketed disinfection products.
OEM Customers
Regulatory clarity for system integrators and equipment providers.
FAQ / Compliance Info
What is required to be compliant under the BPR?
To be compliant with the Biocidal Products Regulation (EU 528/2012), companies must meet two core requirements:
An Article 95 listing for the active substance
A core dossier and product authorization application
What is an Article 95 listing?
Article 95 listing is mandatory for placing biocidal products on the EU market.
It confirms that the active substance supplier is officially listed and compliant with EU regulations.
Why is a core dossier required?
The core dossier contains all technical, efficacy and risk assessment data required for product authorization.
It forms the basis for submitting an application to the evaluating authority and ECHA.
How does ECA Consortium support the process?
ECA Consortium guides you step-by-step through each regulatory requirement and submission.
We support you from initial assessment and documentation to final submission and approval.
Article 95 Listing
Article 95 listing is mandatory for biocidal products on the EU market since 1 September 2015.
This requirement is fulfilled by having an active substance dossier or purchasing a Letter of Access (LoA) from an already listed company.
ECA Consortium is Article 95 listed for active chlorine generated from sodium chloride.
Product Authorization
We generate a core dossier covering all necessary data for product authorization.
The dossier includes precursor, disinfection liquid specifics, use cases, efficacy tests and risk assessments.
We offer Letters of Access for product authorization applications in your own name.
Core Dossier Specifications
The core dossier includes:
– Union authorization under Danish EPA as the evaluating authority
– Active substance: active chlorine (hypochlorous acid/hypochlorite)
– ECA generators with or without membrane
– Precursor compliance (EN 973, EN 14805, EN 16370, EN 16401)
– Five-batch liquid analysis and relevant efficacy tests.
Ready to start your application process?
Tell us about your product and we’ll outline the fastest, most cost-effective compliance route.