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- Title
Forum.
- Abstract
This section offers news briefs related to pharmaceutical medicine as of April 2014. The European Medicines Agency (EMA) is planning to publish full clinical trial data submitted by companies starting January 1, 2014. Adverse drug reaction (ADR) reporting guidance was included by Accreditation Canada in its latest Medication Management Standards. A decision was made by the Irish Medicines Board (IMB) to regulate Ireland's herbal medicines market.
- Subjects
CANADA; IRELAND; EUROPEAN Medicines Agency; DRUG side effects; MEDICATION therapy management; IRELAND. Medicines Board; HERBAL medicine; GOVERNMENT policy
- Publication
Pharmaceutical Medicine, 2013, Vol 27, Issue 2, p129
- ISSN
1178-2595
- Publication type
Article
- DOI
10.1007/s40290-013-0013-7