Last update: May 17th 2013
April 23th 2013

Choose Transparency: A message to the Members...

The Clinical Trial Regulation is currently being discussed. As patients, researchers, doctors, scientists and civil society representatives we would like to draw your attention not only to the dangers it encompasses but also to the opportunities it brings along.

April 09th 2013

Clinical Trials Regulation Protect public...

The International Society of Drug Bulletins issued a statement today to the members of European Parlament to request:

  • support amendments that require the public disclosure of a complete clinical studyreport (CSR) as outlined by ENVI rapporteur MEP...
February 05th 2013

New Proposal for a Regulation on Clinical Trials

The protection of human subjects must be upheld & citizens’ right to information must be strengthened

September 15th 2012

European Medicines Agency and...

On 18 June 2012, the EU Commission published a draft concept paper for public consultation on the “Introduction of fees to be charged by the European Medicines Agency for pharmacovigilance”.

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  15. Article 10: An application for admission must comprise

    1. two copies of each of the last five consecutive issues of the bulletin preceding the date of application. If the issues do not specify the contents in English then a list of these contents, including keywords, shall be sent with the issues;
    2. If appropriate, an English translation of two articles of your bulletin;
    3. a completed application form;
    4. the admission fee (which will be refunded if the application is not accepted).The Committee may request further information to assist it in making its decision.
      Budget of Bulletin Membership fee
      below 30.000 Euro 225 Euro
      over 30.000 Euro 900 Euro
      Developing country 45 Euro (It is possible to apply for exemption when payment is difficult.)

ISDB - International Society of Drug bullettins

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President: president@isdbweb.org
Webmaster: maria.font@ulss20.verona.it

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