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Printed 19/06/2013
Url http://www.dkma.dk/en/tertiary-menu/questions-and-answers
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Questions and answers
Clinical trials - questions and answers
Counterfeit medicines - questions and answers
DKMAnet - Prices & Packages - questions and answers
DKMAnet: Access - questions and answers
DKMAnet: Authorisation of retail sale online - questions and answers
DKMAnet: Clinical trials - questions and answers
DKMAnet: company authorisations - questions and answers
DKMAnet: Follow-up on adverse reaction reports - questions and answers
DKMAnet: Package Leaflets - questions and answers
DKMAnet: reimbursement of medicines - questions and answers
DKMAnet: Security - questions and answers
DKMAnet: Support - questions and answers
DKMAnet: User administration - questions and answers
Generic substitution - questions and answers
GMP requirements for manufacturers of active pharmaceutical ingredients (APIs) - questions and answers
Good Manufacturing Practices (GMP) - questions and answers
Influenza A (H1N1) - questions and answers
Labelling - questions and answers
Medicinal gasses - questions and answers
Pharmacovigilance - questions and answers
Pharmacovigilance legislation – questions and answers
Procedure for authorisation of several qualified persons on section 39 authorisations (new scheme) - questions and answers
Submission of electronic adverse reaction reports from the MAH - questions and answers
Sunset Clause and European Reference Product - questions and answers
The decentralised procedure - questions and answers
Tissues and cells - questions and answers
Variations after 1 January 2010 - questions and answers
Veterinary medicines - questions and answers