News

Key Takeaways from the Recast Drinking Water Directive (DWD)

The recast Drinking Water Directive (EU) 2020/2184 is now in its critical implementation phase, with major deadlines in 2027 and 2028 fast approaching.

Here are the main aspects highlighted in recent expert sessions:

• Risk-based approach (Articles 7 - 10): Proactive safety assessment across the entire supply chain, from catchment to tap.

• Article 11 - Materials in contact with drinking water: All materials must use only substances from the European Positive List (EUPL). From 1 January 2027, a single EU certificate of conformity is required (one test package = EU-wide access). ~600 EUPL entries expire on 31 Dec 2028.

• Notification and Application process: Mandatory Notification of Intentions is now open (1-year validity). Full applications must be submitted at least 18 months before expiry.

• Article 12 - Treatment chemicals & filter media: Strict purity rules and new ECHA/EFSA guidance on transformation products (applies from April 2026).

• Updated parametric values and dynamic Watch List for emerging contaminants (PFAS, endocrine disruptors, microplastics, etc.).

Essential actions now:

• Check your products against the EUPL (watch expiry dates!)

• Verify notifier status on ECHA CHEM

• Consider joint applications with other notifiers

• Start your EU certificate procedure

Need help with EUPL review, notifications, or full DWD compliance?

Contact Alliance Regulatory Limited today:

contact@allianceregulatory.com

ECHA Webinar recording now available: Getting to know the New Chesar Platform

On 2 June 2026, ECHA held a highly informative webinar introducing the new Chesar Platform - the modern successor to Chesar 3 for chemical risk assessments under REACH and biocides legislation.

In the session, ECHA experts presented:

• Key features and scope of the first version of the Chesar Platform

• How it supports chemical safety assessments (REACH) and environmental risk assessments (Biocides)

• Practical guidance on migrating from Chesar 3 to the new platform

• Tips to get started quickly

The webinar is especially useful for registrants, applicants, consultants, and users of Chesar 3 / EUSES.

At Alliance Regulatory, we recommend watching this recording if you are preparing or updating your chemical safety documentation.

Need help with migration, exposure scenarios, or full dossier support?

Contact us: contact@allianceregulatory.com

New BLAC Guidance 2026: Abgaberegelungen nach ChemBiozidDV - Biocide Sales Rules in Germany Explained

Key topics covered include:

• Requirements for the Mandatory Advisory Conversation (Abgabegespräch) - in stores and online shops

• Verification of the buyer’s identity and user category (general public vs professional users)

• Rules for checking that the product will be used correctly and for its intended purpose

• Qualifications (Sachkunde) required for staff selling restricted biocides

• Practical FAQ section addressing many real-world situations

Even if you are not directly active on the German market, this guidance is very instructive on how one of the strictest EU member states interpretes and enforces biocide sales restrictions. 

You can contact us if you want to know how to get the "Professional Expertise" licence (Plant Protection Products, Biocides and Chemicals)

ECHA Webinar 21 May 2026: Preparing Biocides Active Substances in IUCLID and R4BP 3 - Key updates and deadline

Today, the European Chemicals Agency (ECHA) held a highly relevant webinar.

The session focused on key IT developments and practical guidance for preparing active substance dossiers under the Biocidal Products Regulation (BPR). 

Main topics included:

• Recent improvements in the IUCLID format and validation rules

• How to correctly structure and compile data in IUCLID

• Important changes coming into force on 1 July 2026: renewal dossiers must include all data previously used for the initial approval

• Rules and best practices for submissions via R4BP 3

This webinar is particularly useful for manufacturers, authorisation holders, consultants, and anyone preparing new, renewal, or review dossiers for active substances and biocidal products.

At Alliance Regulatory we closely monitor these technical and regulatory developments that directly affect dossier preparation and authorisation strategies. Need a detailed analysis of the impact on your products? Feel free to contact us.

A substantial upgrade to ECHA’s central platform IUCLID for chemical data management under REACH, CLP, BPR, PPP and more

Key Changes in v10

• Major format updates including harmonised OECD templates and new EU-specific fields

• Enhanced support for Biocides (BPR), Plant Protection Products (PPP), microplastics, drinking water, toys, and microorganisms

• Improved user interface and new functionalities for better data quality and interoperability

• Refined validation tools and simplified migration rules

Impact on Your Business

• Existing dossiers must be updated and migrated 

• New data requirements for biocides and PPP submissions 

• Compatibility checks required with your current tools (Chesar, Extractor, etc.) 

• Early preparation is essential to avoid submission delays in 2026 - 2027

Alliance Regulatory is ready to support you 

• Expert review and migration of your IUCLID dossiers 

• Full compliance support for BPR, PPP, REACH & CLP 

• Certified consultant

• Don’t wait until the last minute.

Contact us today → contact@allianceregulatory.com

The Resurgence of Hyalomma lusitanicum in Europe

Public and veterinary health concerns

• Crimean-Congo Haemorrhagic Fever virus (CCHFV): severe viral haemorrhagic fever in humans with high fatality rates; an emerging public-health threat in southern Europe

• Theileria annulata: causes bovine theileriosis (Mediterranean theileriosis), leading to major economic losses in cattle farming

• Coxiella burnetii: responsible for Q fever, a zoonotic disease that can affect both humans (flu-like illness, pneumonia, chronic complications) and livestock

• Various Rickettsia, Anaplasma and Babesia species: associated with spotted fevers, anaplasmosis and babesiosis in humans and animals

Why it matters now

• Increasing presence in France and southern Europe creates urgent need for surveillance and control

• ARL expertise; EFF guidance compliant efficacy testing using locally collected Hyalomma lusitanicum

• Generation of robust, Europe-relevant data for acaricides and topical repellents for humans, pets, horses

Ready to Move Forward?

Contact us at contact@allianceregulatory.com to discuss tailored testing and regulatory solutions for this emerging tick species.

ECHA Bee Risk Guidance for Biocides – Prepare Now!

How We Help

We support your bee risk assessments & dossiers: 

• Portfolio review & strategy (pre- vs post-2026 submissions) 

• Exposure modelling with B-risk tool 

• Bee toxicity testing via our partner EDARA ERF in India – GLP/OECD-compliant, fast, cost-effective, open apiary networks (ideal EU alternative) 

• Full hazard/effect assessment & regulatory integration 

Act Early – Pollinator protection is key for compliance & marketing.

Reach out to us at contact@allianceregulatory.com to exchange on your PT18 needs & EDARA options

Restricted Purchase of Professional Plant Protection Products (PPP) and Biocides

Ensuring Safe & Compliant Use in France and Germany

Safe & Responsible Use: Strict national rules protect health and the environment while ensuring products reach qualified users only.

No Free Access: Professional PPP and biocides cannot be purchased "off the shelf" – certification and verification are essential.

Evolving Regulations: France and Germany implement robust EU frameworks (Regulation 1107/2009 for PPP; BPR 528/2012 for biocides) with national enforcement (Biocidal Products Implementation Regulation: Arrêté «Certibiocide», Arrêté «Certiphyto» and ChemBiozidDV).

We help you navigate certifications, training, & compliance – so you can recommend & sell your products legally & efficiently.

Reach us at contact@allianceregulatory.com

© 2026 Alliance Regulatory. All rights reserved. 

A substantial upgrade to ECHA’s central platform IUCLID for chemical data management under REACH, CLP, BPR, PPP and more