Icelandic Medicines Agency

Navigation

Lyfjastofnun

ima.is

  • Licences
    • Marketing Authorisations
      • Electronic Applications
      • Renewals
      • Variations
      • Labelling - National Requirements
      • Withdrawals - Guidelines
      • RMS Requests
    • Conditions for Marketing
      • Medicinal Products on the Market
      • Medicinal Products not on the Market
      • Agreement regarding labelling of Risk Communication Material
    • Other Authorisations / Registrations
      • Herbal Medicines
      • Homeopathic Medicines
    • Guidelines on Translations and Text Processing
      • Templates and Translations of Standard Sentences
      • Excipients in the Label and Package Leaflet
      • Templates for Veterinary Products
      • Guidelines on Text Processing
      • Vocabulary
    • Guidelines
    • Other Information
    • Clinical Trials
      • Application
      • Fees
      • Substantial amendments
      • Notifications and Reports
      • SUSAR reporting
      • FAQs
      • Approvals for Clinical Trial Applications
      • CTFG/VHP
  • Inspections
    • Pharmacies
      • List of Pharmacies / Pharmacy Outlets
      • Pharmacy Licence
      • Missing Prescriptions
      • Laws and Regulations
    • Manufacturer
      • List of Manufacturers
      • Licences
      • Certificates
      • Laws and Regulations
    • Wholesalers and Distributors
      • List of Wholesalers and Distributors
      • Licences
      • Laws and Regulations
    • Product Classification
      • Laws and Regulations
      • Application
      • Classification of Claims
      • Classification of Substances
        • Medicinal Substances
        • Classified Products
        • Herbs
        • Common Ingredients
        • Vitamins and Minerals
      • Fees
      • FAQs
    • Importation by Individuals of Medicinal Products for Personal Use
      • Laws and Regulations
      • Medicines with MAs
      • OTC Products
      • Herbal Medicines
      • Homeopathic Products
    • Quality Standards
      • GMP
      • GDP
      • GPP
      • GCP
  • Pharmacovigilance
    • General Information
    • Report an adverse drug reaction
    • Legislation
    • EudraVigilance
  • Medical Devices
    • About Medical Devices
    • Medical Device Registration
    • Incident Report for Medical Devices
    • CE Marking
    • Law and regulation on Medical Devices
  • Publications
    • News
      • 2014
      • 2013
      • 2012
      • 2011
      • 2010
      • 2009
      • 2008
    • Lists
      • New Marketed Medicinal Products
        • 2017
        • 2016
        • 2015
        • 2014
        • 2013
        • 2012
        • 2011
        • 2010
      • Withdrawals
        • 2017
        • 2016
        • 2015
        • 2014
        • 2013
    • Forms
    • Annual Reports
    • Articles and Safety Guidance
    • Statistics
      • Key Figures
  • IMA
    • About Icelandic Medicines Agency
      • E-mail addresses
      • Statutory Function, Mission Statement and Core Values
      • Summary
      • Organisation Chart
        • Licensing Unit
        • Information and Education
        • Inspections Unit
        • Finances
        • Legal Affairs
        • Quality Management
      • Starfsmannastefna
      • Upplýsingaskylda
      • Location
      • Gender Equality Policy
      • Code of Ethics
      • Service Hours
      • Disclaimer and copyright
    • The Pharmaceutical Committee
    • Quality and Performance
      • BEMA
      • BSC
      • Quality
    • Laws and Regulations
    • Fees
    • International relations
    • FAQs
    • Contact Us
      • Suggestions/Complaints
    • Links
You are here: Home > Sitemap

ima.is

  • Licences
    • Marketing Authorisations
    • Conditions for Marketing
    • Other Authorisations / Registrations
    • Guidelines on Translations and Text Processing
    • Other Information
    • Clinical Trials
  • Inspections
    • Pharmacies
    • Manufacturer
    • Wholesalers and Distributors
    • Product Classification
    • Importation by Individuals of Medicinal Products for Personal Use
    • Quality Standards
  • Pharmacovigilance
    • General Information
    • Report an adverse drug reaction
    • Legislation
    • EudraVigilance
  • Medical Devices
    • About Medical Devices
    • Medical Device Registration
    • Incident Report for Medical Devices
    • CE Marking
    • Law and regulation on Medical Devices
  • Publications
    • News
    • Lists
    • Forms
    • Annual Reports
    • Articles and Safety Guidance
    • Statistics
  • IMA
    • About Icelandic Medicines Agency
    • The Pharmaceutical Committee
    • Quality and Performance
    • Laws and Regulations
    • Fees
    • International relations
    • FAQs
    • Contact Us
    • Links

Efraval

  • Sitemap
  • Contact us
  • Icelandic

Leita á vefnum

  • Icelandic Medicines Agency (IMA)

    Vínlandsleið 14, 113 Reykjavík - Phone 520 2100 - Fax 561 2170
    Kt.: 670900-2740 - ima@ima.is
    Disclaimer and copyright

  • Opening Hours

    8:30 - 16:00            

    Monday to Friday

    Holidays 2017

  • Follow us on Twitter

    • @lyfjastofnun

Page style:

  • Use my settings
This website is built with Eplica CMS