The role and purpose of the POC Manufacturing of Medical Devices Steering Committee and maintaining active channels of communication to facilitate the timely sharing of information between the Steering Committee and the Working Group.
The importance of leveraging the collective experience of Working Group participants and feedback from their members to ensure any potential options/solutions put forward by the Steering Committee are fit-for-purpose, focus on patient safety and do not introduce any unnecessary regulatory burden.
What the roles and responsibilities of dental practitioners and professionals in the manufacture and supply chain including:
skills, training, and qualifications
potential regulatory arrangements for non-Ahpra registered dental professionals
Ahpra and the National Boards’ shared Code of Conduct
standards for dental practitioner registration in mitigating the risks associated with manufacture and supply of medical devices at the POC
Administrative, resourcing, and cost impacts for dental laboratories in complying with the requirements for documenting Quality Management Systems in their facilities.