Adverse drug reaction system
Finnish Medicines Agency Fimea is launching a procurement for a single new system to replace the currently separate IT systems for recording adverse drug reactions on human and veterinary medicines.
The system shall cover the adverse reaction records submitted by health care professionals and ordinary citizens, adverse reaction records submitted by the pharmaceutical industry, storage of records submitted on paper, processing and reporting the records for the European Medicines Agency, reception of adverse reaction records from the European Medicines Agency, generation of reports, and, as an option, signal detection from the accumulated material.
More details are provided in the attachment.
Attachments can be ordered from Fimea's registrars office via email:
kirjaamo@fimea.fi
Määräaika
Tarjousten vastaanottamisen määräaika oli 2016-01-11.
Hankinta julkaistiin 2015-12-08.
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| 2015-12-08
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| 2016-10-28
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