European Medicines Agency policy on access to documents (related to medicinal products for human and veterinary use)

Author (Corporate)
Publication Date 2010
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The European Medicines Agency (EMA), on 30 November 2010, published its new policy on access to documents relating to medicines for human and veterinary use. The new policy is part of the Agency’s response to increasing public demand for more openness and transparency.
Source Link Link to Main Source http://www.ema.europa.eu/docs/en_GB/document_library/Other/2010/11/WC500099473.pdf
Related Links
EMA: Press Release: EMA/718259/2010 (30.11.10): European Medicines Agency widens public access to documents http://www.ema.europa.eu/docs/en_GB/document_library/Press_release/2010/11/WC500099468.pdf
EMA: Output of the European Medicines Agency policy on access to documents related to medicinal products for human and veterinary use http://www.ema.europa.eu/docs/en_GB/document_library/Regulatory_and_procedural_guideline/2010/11/WC500099472.pdf
European Ombudsman: Press Release: EO/10/23 (1.12.10): Ombudsman applauds European Medicines Agency's adoption of new transparency policy http://europa.eu/rapid/pressReleasesAction.do?reference=EO/10/23&format=HTML&aged=0&language=EN&guiLanguage=en
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