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Ireland · Question · written

PQ 687

687. Deputy Tom Fleming asked the Minister for Health his plans to introduce legislation requiring pharmaceutical companies to publish tests and clinical trials to ensure all trials are registered, a summary of results is made publicly available within one year of completion of the trial and full clinical study reports are made available, especially in view of the ongoing concerns of the severe adverse affects of the human papilloma virus-cervical cancer vaccine; and if he will make a statement on the matter. [37540/15]

askedIreland· Dáil Éireann· EN

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3 November 2015

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written

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3 November 2015

Summary

687. Deputy Tom Fleming asked the Minister for Health his plans to introduce legislation requiring pharmaceutical companies to publish tests and clinical trials to ensure all trials are registered, a summary of results is made publicly available within one year of completion of the trial and full clinical study reports are made available, especially in view of the ongoing concerns of the severe adverse affects of the human papilloma virus-cervical cancer vaccine; and if he will make a statement on the matter. [37540/15]

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Clinical Trials

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