Marketing authorization procedures in eu
A decade of eCTD - Time to rejuvenate!
C5 second medical_use_patents_presentation_29_january_2014
What can we learn from developing medicines information for patients?
REGULATION (EC) No 1901/2006 of 12 December 2006 on medicinal products for paediatric use Article 45 and more… Christer Backman CMD(h) Sweden.
IPhVWP Polish Presidency, Warsaw October 6 th 2011 Almath Spooner Irish Medicines Board Monitoring the outcome of risk minimisation activities.
Principle of Thailand Medicine Reclassification Guidelines Mrs. Nantarat Sukrod Bureau of Drug Control Food and Drug Administration September 17, 2015.
REGULATION (EC) No 1901/2006 of 12 December 2006 on medicinal products for paediatric use
STRUCTURE AND PROCESS OF PERIODIC SAFETY UPDATE REPORTING SYSTEM MEDICINES IN KENYA KIOGORA MWITI GATIMBU REG NO.U51/64042/2013 M.PHARM-EPIVIGIL 24 TH.
Slide 1 of 18D.K. Mubangizi, Dar Es Salaam Sept. 2007 Training Workshop for Evaluators from National Medicines Regulatory Authorities in East African Community.