Reactions Weekly

, Volume 1673, Issue 1, pp 2–2 | Cite as

DKMA introduces new practice for follow-up on ADR reports

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Reference

  1. Danish Medicines Agency. New practice for the processing of pharmaceutical companies' requests for follow-up information on adverse reaction reports. Internet Document : 22 Sep 2017. Available from: URL: https://laegemiddelstyrelsen.dk/en/sideeffects/side-effects-from-medicines/companies-reporting-of-side-effects/follow-up/

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© Springer International Publishing AG 2017

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