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  •   For public
  •   Current events
  •   Databases and registers
  •   Development and HTA
  •   Marketing authorisations
  •   Medical devices
  •   Pharmaceutical safety and information
  •   Pharmacies
  •   Supervision
  •   Veterinary
    • Special permits for compassionate use
      • Applying for special permit
      • FAQ
        • A Questions and answers on how to fill in the form
        • B Questions and answers regarding the technical aspects of permit application
        • C Questions and answers regarding the decision and the processing of the application
        • D Other questions and answers
      • Lists of veterinary medicinal products
    • Adverse effects
    • Consumption of veterinary antimicrobials
    • Clinical trials on veterinary medicinal products
    • Withdrawal period and MRL
    • Private import
    • Marketing authorisation procedures
  •   About us
  • Front page
  • Veterinary
  • Special permits for compassionate use
  • FAQ
  • A Questions and answers on how to fill in the form

A Questions and answers on how to fill in the form

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Frequently asked questions

  • Where can I find information on which pharmaceutical wholesaler to turn to for a specific medicinal product?
  • What should I take into account when assessing the quantity of the medicinal product needed?
  • Where can I find the information required to fill in section “Information on the medicinal product”?
  • Is detailed information required in the Target species section, or is a more general description, such as Reptile, sufficient?
  • Should all therapeutic indications be listed if the medicinal product is an anti-microbial or an anti-parasite drug?
  • What information is required under Place of use?
  • Should I provide grounds for use if the product has been granted a marketing authorisation in Finland but has not been launched on the market?
  • Why is it necessary to explain the reasons for which a product with marketing authorisation cannot be used?
  • I am a Bachelor of Veterinary Medicine. How should I sign applications?
  • How should I fill in the application for a special permit when the medicinal product is used for the ex tempore manufacture of a medicine?
  • How should I indicate the quantity?
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