Biocides / Pesticides

We provide a complete regulatory and scientific partnership, offering expert advice and full dossier preparation for active substance approval and product authorisations to ensure your biocides and treated articles can be legally marketed globally.

What is it?

Biocides are chemical substances or mixtures, like disinfectants, antimicrobials, preservatives, and insect repellents, that are designed to control harmful organisms (pests, bacteria, viruses) by chemical or biological means. The definition, categorisation, the regulations and competent authorities responsible for controlling them can differ globally.

Navigating the complex global regulations for biocides and pesticides can feel overwhelming. These regulations are designed to protect human health and the environment from the potential risks associated with such biocides and their uses, but they create significant challenges for companies trying to bring their essential products to market or in keeping them compliant.

We help you meet these challenging requirements across the globe, ensuring your biocidal products, treated articles, and pesticides are correctly classified, authorized, and compliant, so you can maintain market access and focus on your business goals.

For example the EU and UK this would require compliance with the Biocidal Product Regulation (BPR) and the necessary processes involved specifically to your company's position.

For the US and Canada this would be determined based on the actives used and the use and claims of the particular product. The authorities and regulations governing the requirements differ also based on this information.

For Turkey, this would require compliance with Turkey BPR.

What you get

Tailored approach and Strategic Advantage

We provide advice that is focused on adding value to your product and helping you maintain a competitive edge by ensuring compliance.

Guaranteed Market Access

We support you in meeting all requirements to ensure your biocidal products can be legally placed on your target markets.

Compliance Certainty

Our expertise minimizes the risk of non-compliance and safeguards product marketability.

Efficient Data Strategy

We leverage non-testing strategies to reduce time and costs associated with extensive new testing.

What we offer

We possess over a decade of experience to provide end-to-end regulatory support for biocides whether that be for the active substance or for the product for which it is incorporated. Our services include the comprehensive preparation of active substance/ingredient approval and product authorisation dossiers, expert liaison with competent authorities,scientific services and strategic advice to ensure a clear pathway for global market access.

We offer comprehensive services for the biocides industry, covering the entire product lifecycle from initial active substance approval through to product formulation, market placement, and continued compliance. Our offerings include:

Biocide Scoping Assessments & Representation Services

We determine whether your product or treated article falls under the scope of key regulations (such as the EU or GB BPR) and clarify your specific regulatory obligations. In addition, we can act as your Article 95 Representative or Authorisation Holder, providing the necessary representation to support compliance and market access.

Active Substance Approval & Product Authorisation

We prepare, manage, and submit full dossiers for the approval of active substances and the authorisation of biocidal products, including for the EU Biocidal Product Families, Union and Simplified Authorisation procedures.

Technical Data & Testing Strategies

We conduct Data Gap Analysis, manage the commissioning of new studies (e.g.Efficacy) via our trusted network, and develop Intelligent Testing Strategies (preferring in vitro to new in vivo tests where possible).

Hazard Communication

We ensure compliance with Classification, Labelling, and Packaging (CLP) requirements and other biocide related labelling requirements, including label reviews and the production of compliant Safety Data Sheets (SDS).

Our Process

Scope and Strategy

We begin with an assessment of your product information to confirm the regulatory status of your product and develop a robust, tailored regulatory strategy to ensure market access. This initial assessment can support businesses in their R and D phases to decipher whether there are any regulatory aspects to consider and to help give companies the knowledge gain to make informed business decisions

CA clarification

Communicate with Competent authorities were required to confirm next steps.

Data Analysis and Generation

We perform a Data Gap Analysis review including any existing data, required testing strategies or commissioning of new studies (e.g. efficacy) to gather all necessary data to support your submission.

Dossier / Application Preparation and Submission

Our team prepares the full Active Substance Approval or Product Authorisation dossier in the required format and submits it to the relevant competent authorities.

Post-Submission Support

We manage communications with regulatory authorities and provide ongoing expert advice until your product approval is secured.

Related Services

Hazard Communication

ED assessment

Scientific services

REACH services

Product portfolio audits

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