./
en
Mandatory Problem Reporting (Incident)
Issues related to technical requirements, documents, or regulatory information requirements for each MPR module report
Field Corrective Action (FCA)
Issues related to technical requirements, documents, or regulatory information requirements for each FCA module report
Recall
Issues related to technical requirements, documents, or regulatory information requirements for each Recall module report
User Management
System issue
Issues impacting service functionality, structure, components, and causing confusion and system application challenges of each module in the system
© Copyright 2022 Medical Device Authority, Ministry of Health. All Right Reserved.