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laegemiddelstyrelsen.dk – Forside - Sundhedsstyrelsen

UNIGEL brystimplantater er korrekt certificeret 16 Aug 2013 | 06:25 pm

De tjekkiske myndigheder har meddelt, at det bemyndigede organ ITC efter de tjekkiske myndigheders vurdering har certificeret UNIGEL® brystimplantater korrekt og i henhold til gældende regler. Konklus...

Sundhedsstyrelsens rapport om NSAID’er – forbruget, indberettede formodede bivirkninger og utilsigtede hændelser 16 Aug 2013 | 03:59 pm

Sundhedsstyrelsen har lavet en rapport, der gennemgår forbrug, indberettede formodede bivirkninger og utilsigtede hændelser ved non-steroide anti-inflammatoriske lægemidler (NSAID). Stigning i forbru...

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Safety Concerns on the Use of Rosiglitazone nafdac.gov.ng 19 Nov 2010 | 12:28 am

The recent regulatory actions by the European Medicines Agency (EMA) and the United States Food and Drug Administration (USFDA) regarding Rosiglitazone-containing medicines marketed by GlaxoSmithKline...

European watchdog warns about dangers of Acomplia weightlossdrugs.bloghi.com 23 Jul 2007 | 10:12 am

The European Medicines Agency has warned consumers that the weight loss drug Acomplia heightens the risk of suicide among those taking anti-depressants. The agency wants stronger warnings placed on t...

EMA: Use modafinil only for narcolepsy pharmacologycorner.com 22 Oct 2010 | 02:35 pm

The European Medicines Agency recommended restricting the use of modafinil for narcolepsy only. “The European Medicines Agency has recommended restricting the use of modafinil-containing medicines. T...

Statistics On Drug Testing lesdragons.forumpro.fr 1 Aug 2011 | 12:40 am

Statistics On Drug Selling It was October 2008, where European Medicines Agency concluded that benefits of Acomplia no longer outweighed its risks and it is recommended to be withdrawed in the market....

VVUS, CRWE, JOSB, RPTP - CRWEPicks.com Stock Report! VIVUS Inc., Crown Equity Holdings Inc., JoS. A. Bank Clothiers Inc., Raptor Pharmaceutical Corp. crwepickz.posterous.com 27 Mar 2012 | 02:45 am

VIVUS, Inc. (Nasdaq:VVUS) reported that a Marketing Authorization Application (MAA) has been accepted by the European Medicines Agency (EMA) for the review of avanafil, its investigational drug for th...

THE PARTY IS OVER medicineagency.com 10 Mar 2011 | 08:36 am

[ March 19, 2011 8:00 pm to March 20, 2011 12:00 am. ] Dear Friends, Family, and Colleagues: After nearly two wonderful years, MEDICINE AGENCY will be closing the doors to its San Francisco location...

Macaframa Crosstown Traffic medicineagency.com 26 Feb 2011 | 11:35 am

[ March 5, 2011; 7:00 pm; ] Next weekend Macaframa is hosting a fixed-only cyclocross inspired race downtown and photo exhibition at Medicine Agency to celebrate the new Maca Bike and launch our new ...

Albireo Receives Orphan Drug Designation for its Severe Liver Diseases treatment europe-health-care.eu 24 Jul 2012 | 03:23 pm

Albireo AB, a Swedish biopharmaceutical company, today announced that the European Medicines Agency Committee for Orphan Medicinal Products (COMP) has issued a positive opinion on an application for o...

Astex Pharmaceuticals Receives a Positive Regulatory Recommendation in the EU for its Acute Myeloid Leukemia treatment europe-health-care.eu 20 Jul 2012 | 11:19 pm

Astex Pharmaceuticals today announced that Janssen-Cilag International NV was notified that the Committee for Medical Products for Human Use (CHMP) of the European Medicines Agency (EMA) granted a pos...

UniQure’s gene therapy for lipoprotein lipase deficiency recommended for approval as Orphan Drug europe-health-care.eu 20 Jul 2012 | 07:54 pm

uniQure announced today that the European Medicines Agency’s (EMA)  Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion that recommends marketing authorization of Glybe...

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