Devices In Finland Now Supervised By Medicines Regulator
Fimea believes that transferring supervision duties for medical devices to under its remit will concentrate its expertise related to the quality, efficacy and safety of medicines and devices, and result in synergy benefits.
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Members of Italian industry body Confindustria Dispositivi Medici should insert a suitable transparency clause in their agreements with health care professionals, says law firm Osborne Clarke, after the trade association introduced a new requirement relating to payments to HPCs.