Biocidal products are divided into 22 product types. The following product types are classified as veterinary biocides: 3 (veterinary hygiene), 4 (food and feed), 14 (rodenticides), 18 (insecticides, acaricides and other arthropod control products), 19 (repellents and attractants) and 22 (embalming and taxidermy fluids). These are products used for veterinary hygiene purposes and for the disinfection of equipment, containers, and surfaces related to the keeping or transport of animals, as well as for rodent control.
Depending on their exact purpose and composition, veterinary biocidal products can be dangerous to the environment, human health or even life. They are also classified as chemical substances and mixtures, and biocides are subject to multi-layered regulatory requirements.
The regulation of veterinary biocides is based on both the BPR Regulation (EU Regulation No. 528/2012) and the CLP Regulation, and additional legislation, such as the Detergents Regulation, may also apply to specific product functions (e.g., cleaning).
In order to legally and smoothly supply a product to any EU market, it is critically important to properly assess the requirements applicable to a specific product. INTRA VIRES experts will not only provide clear conclusions, but also prepare a specific action plan that will help you avoid costly mistakes and smoothly authorise, notify, and label your product.
The most common questions and topics we advise on:
- Is it necessary to authorise the product in each country separately?
- How long are biocidal product authorisation certificates valid?
- What efficacy studies are required to authorise a veterinary biocidal product?
- Who are the possible suppliers of active substances for my product?
- Which laboratory can perform efficacy studies?
- Can you prepare a safety data sheet for a veterinary biocidal product?
- Where can I find a list of authorized veterinary biocidal products?
- How long does the authorization process take and what documents are required?
- What is the applicable amount of the state fee?
- Is it necessary to generate a UFI code and notify the mixture to ECHA?
- Is it necessary to notify the mixture/substance via the IS AIVIKS system?
Organisation of efficacy studies for veterinary biocidal products
Every product that claims to have a biocidal (antiviral, antibacterial, etc.) effect must have test protocols to support this claim. The tests are necessary both for product authorization and to substantiate the claims made on the packaging and in advertising content. Taking into account the purpose of the product and your needs, INTRA VIRES experts will strategically assess the need for studies, select appropriate laboratories, and ensure that the studies comply with EU requirements.
Why is it worth contacting experts?
The regulation of veterinary biocidal products is a dynamic and complex area. An inappropriate strategy, poor-quality documentation, or failure to meet requirements can delay the product’s entry into the market, result in additional costs, and lead to legal liability. Consultations on the regulation of veterinary biocidal products will help you avoid these risks and properly assess the applicable requirements. We will also share best practices that will help you get your product on the right shelf.
Countries where we offer this service
Biocidal product authorisation is carried out in accordance with Regulation (EU) No. 528/212 on biocidal products. National legislation also applies to the authorisation process. We advise clients in Lithuania, Latvia, Estonia and other EU countries (subject to separate agreement).
