Animal nutrition
At Pharmanager Development, we leverage our expertise to support our clients in the development and market entry of their animal nutrition products. we ensure regulatory compliance throughout their lifecycle, guaranteeing safety, quality, and efficacy. whether for new product development, labeling, or regulatory dossier submission, we provide comprehensive and tailored assistance.
Labeling and communication compliance verification
We analyze your labels and communication materials to ensure they comply with legal requirements while enhancing the value of your products for consumers.
Formula compliance verification
We assess your formulations to ensure they comply with regulatory standards, using only authorized and suitable ingredients for their intended use.
Preparation of a scientific dossier to substantiate claims
We prepare comprehensive dossiers, including literature reviews and, if necessary, specific studies to substantiate your nutritional claims.
Development of an animal feed product
We assist you in formulating and developing new products tailored to nutritional needs and market expectations in Europe and internationally.
Market entry of a new additive or a new use
We ensure the compliance of your additives or new applications in accordance with regulations (EC) no 1831/2003 and (EC) no 429/2008, to secure their authorization.
Regulatory and scientific monitoring
We continuously monitor legislative and scientific developments in Europe and internationally to ensure the compliance and innovation of your products.
Pharmanager development assists you in
we guide you through every stage of your product lifecycle, from conception to market launch, leveraging our regulatory and scientific expertise while ensuring compliance with legal requirements.
whether for development, formulation validation, or claim assessment, we provide tailored assistance, ensuring compliance for labeling and technical dossiers.
with ongoing regulatory monitoring, we maximize your chances of success by anticipating legislative changes and addressing the challenges of the animal nutrition sector.
Discover our case studies
Do you want to enhance your knowledge of animal nutrition regulations?
Our answers to your questions
Do I need to declare my animal feed products on Compl’Alim?
No, unlike food supplements for human consumption, there is no requirement to declare products to the competent authority under the regulation.
How does EFSA contribute to the safety assessment of feed additives?
EFSA’s Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) provides independent scientific advice on the safety and efficacy of feed additives. The panel evaluates the potential risks to target species, users, consumers of products of animal origin, and the environment. Their assessments are essential for the authorization process of feed additives within the EU.
What is the role of the International Feed Industry Federation (IFIF) in promoting animal health through nutrition?
The International Feed Industry Federation (IFIF) focuses on nutritional innovation to promote animal health and welfare. Their work aims to demonstrate how animal nutrition contributes to animal health and welfare, including efforts to contain Antimicrobial Resistance (AMR). IFIF’s initiatives support the industry in adopting practices that enhance animal health through improved nutrition.
How do regulatory frameworks address the use of novel ingredients, such as insects, in animal feed?
The use of novel ingredients in animal feed, such as insects, is subject to specific regulatory frameworks to ensure safety and efficacy. In the European Union, the use of insects in feed was previously prohibited but has been revised to allow certain insect products in fish feed. Regulations require that these novel ingredients undergo safety assessments and meet specific standards before being approved for use in animal feed.