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Aandeel Pharming Group AEX:PHARM.NL, NL0010391025

Laatste koers (eur) Verschil Volume
0,948   +0,055   (+6,10%) Dagrange 0,891 - 0,950 15.069.470   Gem. (3M) 6,4M

21 feb slotkoers pharming

155 Posts
Pagina: «« 1 ... 3 4 5 6 7 8 | Laatste | Omlaag ↓
  1. forum rang 10 voda 21 februari 2014 17:43
    quote:

    PharmOptimist schreef op 21 februari 2014 17:40:

    Volgens mij is deze man de winnaar:

    0,595 : schoutenjr
    Geinig!

    quote:

    schoutenjr schreef op 20 feb 2014 om 22:41:

    Tja ik bn nog een leek op dit forum aangezien mijn beroep bouwvakker is haha. En ben nog jong

    En toch een goed rendement gehaald in vier maanden ong 80 procent

    Kom er maar in met je advies voor volgende week :-)
  2. [verwijderd] 21 februari 2014 18:34
    quote:

    tulip schreef op 21 februari 2014 18:31:

    Zo zien we maar weer eens vandaag dat het aandeel pharming heet, en er ook gekke dingen kunnen gebeuren. Er zullen nog wel meer correcties volgen op weg naar16 april naar het ging wel snel down vanmiddag. Toch maar moed blijven houden. Goed weekend allemaal.
    Hetzelfde als hier, vanmorgen gekocht op 0.657 en een aardig pakketje ook zelfs.

    Fingers crossed komende weken
  3. netweblady 21 februari 2014 18:43
    WEDNESDAY Feb. 19, 2014, 2014 -- The U.S. Food and Drug Administration and the European Medicines Agency (EMA) have set-up a new 'cluster' on pharmacovigilance (medicine safety) topics. Clusters are regular collaborative meetings between the EMA and regulators outside of the European Union, which focus on specific topic areas that have been identified as requiring an intensified exchange of information and collaboration. Building on the experience of previous regular videoconferences between the FDA and the EMA in this area and on the recent creation of the EMA’s Pharmacovigilance Risk Assessment Committee, this cluster will provide a forum for a more systematic and focused exchange of information on the safety of medicines.

    The FDA and the EMA have already set-up such clusters to discuss issues related to biosimilars, medicines to treat cancer, orphan medicines, medicines for children, blood-based products, among other topics. Health Canada and the Japanese Pharmaceuticals and Medical Devices Agency are also involved in some of these clusters.

    “The work of protecting the health and safety of the American people cannot be done in isolation,” says Janet Woodcock, Director, M.D., director of the FDA’s Center for Drug Evaluation and Research. “It is part of a larger collaborative global effort between the FDA and its international regulatory partners to ensure the health and safety of all our citizens.”

    As part of the new cluster, discussions on shared pharmacovigilance issues will now take place between the agencies on a monthly basis by teleconference. This increased degree of interaction will allow the agencies to work swiftly in the area of the safety of medicines and to coordinate communication activities. The creation of this cluster is the latest step in the FDA’s and the EMA’s broader approach to expand and reinforce international collaboration.

    “In an increasingly globalised pharmaceutical market, collaboration between medicines’ regulators is essential,” explains Guido Rasi, the EMA’s Executive Director. “Medicines’ regulators are inter-dependent: any action taken in one territory has repercussions on the rest of the world. International cooperation is a key area of work for the agency.”

    This type of collaborative effort is important for ensuring the safety and quality of medicines distributed to consumers throughout the globe. The new cluster will help medicines’ regulators harmonize efforts to keep medicines safe, regardless of location.

    Canadian and Japanese regulatory authorities will participate in the meetings of the cluster on pharmacovigilance as observers. The information exchange is covered by confidentiality arrangements between the FDA and the other participants.

    Source: FDA

    Posted: February 2014
155 Posts
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