Veterinary products
Feed legislation
Medicated feeding stuffs
Feed additives

How KÆLTIA’s team can help you?

  • Strategic advice and Guidance.
  • Data gap analysis: data available vs data required.
  • Preliminary risk assessments.
  • Preparation of EU dossiers for authorisation
    and renewal.
  • Preparation of EU Mutual Recognition applications.
  • Preparation of National registration dossiers in Europe (during the transitional period).
  • Preparation of National registration dossiers in North and South America, Asia, Australia and Africa.
  • Technical equivalence dossier for new active substance source.
  • Toxicological, environmental and consumer risk assessments.
  • Modelling and development of exposure scenarios.
  • Expert judgments to avoid unnecessary testing.
  • ‘Read-across’ and ‘QSARs’.
  • Study commissioning and monitoring with accredited laboratories.
  • Follow-up of the registration process until the product approval.
  • CONSORTIA coordination for REACH, Biocides and Plant Protection Products.
  • Data sharing negotiations.
  • Classification of substances and mixtures according to CLP.
  • Preparation of SDS, e-SDS and commercial labels according to local requirements.
  • Liaison with the Authorities.
  • Only Representative and Third Party Representative services.
  • Literature search.