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IMA
About Icelandic Medicines Agency
Statutory Function, Mission Statement and Core Values
Organisation Chart
E-mail addresses
Summary
Code of Ethics
Location
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Medicine Consumption and Turnover
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Quality and Performance
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Quality
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The Pharmaceutical Committee
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Legislation
Adverse Drug Reaction Report (ADRs)
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Importation by Individuals of Medicinal Products for Personal Use
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Homeopathic Products
Licences
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Electronic Applications
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Withdrawals - Guidelines
Timetable for Handling MAs and Variations
Labelling - National Requirements
RMS Requests
Other Authorisations/Registrations
Licences for Parallel Import
Guidelines on Translations and Text Processing
Templates and Translations of Standard Sentences
Templates (Veterinary Products)
Excipents in the Label and Package Leaflet
Guidelines on Text Processing
Vocabulary
Terminology
Standard Terms
Short Standard Terms
Routes of Administration
Containers
Guidelines-Electronic applications
Other Information
Medicinal Product Information (SPC)
Pharmacovigilance
Consumers
Spontaneus Reporting (ADRs)
Pharmacovigilance Druglist
Legislation
What is to be reported
Spontaneus Reporting (ADRs)
EudraVigilance
FAQs
Marketing Authorisation Holders (MAH)
Letter to MAHs
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Medicines under special surveillance
Healthcare Professionals
Medicines under special surveillance
Spontaneous Reporting (ADRs)
What happens to reports
Legislation
Clinical Trials
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FAQs
Product Classification
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Classification of Substances
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FAQs
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