Quality and manufacturing practice
Responsibilities across manufacture, supply, product change and documentation.
about
IAHPM organises technical participation around questions that matter across health-product manufacturing.
Responsibilities across manufacture, supply, product change and documentation.
Interpretation of performance evidence and the statements made about products.
Product data definitions, handovers and the relationship between devices and software.
A working group requires a written remit, named coordination, a contribution plan and a review point. Its assignment should identify a practical output, such as a briefing, comparison of methods or professional discussion guide.
A participation enquiry should identify your organisation, relevant experience, the question you propose to address and the contribution you can make. Participation and access to restricted discussion are agreed separately from membership.
Contributors disclose relevant interests and respect the agreed scope. Draft discussion is not an Association position. Public outputs follow the editorial policy and remain linked to their supporting material.