Home » EU’s Cross-Border Directive Gives Devicemakers More Voice on HTA
EU’s Cross-Border Directive Gives Devicemakers More Voice on HTA
February 9, 2011
EU devicemakers are welcoming Parliament’s vote last month on the Cross-Border Healthcare Directive, which will ensure industry’s voice is heard in the development of health technology assessments (HTAs).
To View This Article:
Subscribe To International Medical Device Regulatory Monitor