"Our news". nordic.cochrane.org. Archived from the original on 31 August 2017. Retrieved 21 August 2019.
europa.eu
ema.europa.eu
Set up by EC Regulation No. 2309/93 as the European Agency for the Evaluation of Medicinal Products, and renamed by EC Regulation No. 726/2004 to the European Medicines Agency, it had the acronym EMEA until December 2009. The European Medicines Agency does not call itself EMA either – it currently has no official acronym but may reconsider if EMA becomes commonly accepted (see communication on new visual identityبایگانیشده در ۱ ژوئن ۲۰۱۰ توسط Wayback Machine and logoبایگانیشده در ۲۵ دسامبر ۲۰۰۹ توسط Wayback Machine).
Sherwood, Ted (16 April 2008). "Generic Drugs: Overview of ANDA Review Process"(PDF). CDER Forum for International Drug Regulatory Authorities. Food and Drug Administration, Office of Pharmaceutical Science. Retrieved 30 January 2010.
ft.dk
Louise Brinth: Responsum to Assessment Report on HPV-vaccines released by EMA November 26th 2015., online (PDF; 1,3 MB)
Set up by EC Regulation No. 2309/93 as the European Agency for the Evaluation of Medicinal Products, and renamed by EC Regulation No. 726/2004 to the European Medicines Agency, it had the acronym EMEA until December 2009. The European Medicines Agency does not call itself EMA either – it currently has no official acronym but may reconsider if EMA becomes commonly accepted (see communication on new visual identityبایگانیشده در ۱ ژوئن ۲۰۱۰ توسط Wayback Machine and logoبایگانیشده در ۲۵ دسامبر ۲۰۰۹ توسط Wayback Machine).
