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February 10, 2017
EMA announces that the European Union’s PAS Register has received its 1000th upload.
Pharmaceutical Technology spoke with Tommy Fanning, head of biopharmaceuticals for IDA Ireland, to get a perspective on how Brexit may affect the pharmaceutical industry.
February 02, 2017
Early-access schemes aim to make medicines available to patients faster but the regulatory framework remains unclear especially for biologics that involve complex manufacturing.
January 27, 2017
The agency recommended approval of a total of eight drugs at its January 2017 meeting, two of which are biosimilars.
January 19, 2017
The agency published an overview of marketing authorizations made in 2016.
January 18, 2017
EDQM outlines the steps it will take to implement the ICH Q3D guideline on elemental impurities.
January 01, 2017
How involved should HTA bodies be in assessing cost effectiveness and reimbursements?
December 16, 2016
The agency announces that 81 medicines overall were recommended in 2016.
December 02, 2016
Better co-ordination within and between regions is needed to improve the global regulation of medicines, according to the European Medicines Agency.
November 11, 2016
The agency recommended nine drugs including treatments for diabetes, hepatitis B, and HIV.