EC rapport activiteiten voor verbeteren veiligheid medicijnen
The Commission published a report on activities by Member States and the European Medicines Agency (EMA), to monitor the safety of medicines throughout their life cycle as foreseen by the 2010 amendment of the EU legislation from 2001 and 2004. The report describes the activities of the collaborative EU system for monitoring and controlling the safety of human medicines since the new legislation came into effect in 2012 until July 2015.
The report concludes that the European pharmacovigilance network is an example of successful cooperation at EU level which directly benefits patients. Work is underway on improving the system’s infrastructure (EU Public Health News, 8 augustus 2016).
Klik hier voor het volledige nieuwsbericht.
Klik hier om het rapport van de commissie te downloaden (376 kB).
Klik hier voor meer informatie over het NVC-project Pharmaceutical Packaging Innovation.
Klik hier voor meer informatie over de NVC E-Course Pharmaceutical Packaging.
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