1.Medical Device development and lifecycle management under the MDR and IVDR
Requisitos de conclusão
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1. Medical Device development and lifecycle management under the MDR and IVDR
1.3. Device production phase
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- further expansion of the QMS, e.g.,
- a batch release process
- Quality Control (QC) procedures
- change control processes
- complaint management processes
- further expansion of the QMS, e.g.,