Aussies In-House, Commercial IVDs Should Meet Same Conformity Standards
Australia Opens Door to CE Mark for ‘Routine’ Medical Devices
Devicemakers Push for Lesser TGA Role in Conformity Assessments
Report Shows Strides in Implementing EU Joint Action Plan on Devices
Industry Seeks More Substantive Reforms in Scrutiny of Notified Bodies
New Zealand, EU Agree to Recognize Conformity Assessments, GMP Audits
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