Quality First International

Quality First International expresses concern at the lack of proper scrutiny of clinical data and statutory obligations

The amendments to Council Directive 93/42/EEC relating to clinical data, which will come into force on 21 March 2010, are already affecting manufacturers of medical devices in Europe. Quality First International is alerting medtech companies

Regulatory alert: MANDATORY REGISTRATION OF CLASS I, IIa, IIb and III MEDICAL DEVICES in ITALY – Quality First International alerts clients and medtech companies