Inventory
Document
Project
Configuration
Incident
Change
CAPA
Knowledge
Training
Test
ComplaintProviding a complete lifecycle
Provides the functionality of creating, investigating, tracking, and closing deviations for IT systems, processes, and/or procedures. Corrective Action / Preventive Action (CAPA) must be planned and approved before they are implemented to close out a Deviation.
Ensures full traceability
The Deviation is linked to the Inventory, and at the same time linked back to the trigger of deviation and forward to the CAPA associated with the deviation. This single solution ensures full traceability. The Deviation Management workflow within MyBlueLabel are as follows: Raise Deviation – Observation, Investigation, Review Deviation (CAPA) Internal, Review Deviation (CAPA) Independent,
Approval for Realization, and Deviation Approved.
Document deviation
With the module your company can follow up and correct non-compliant incidents and activities. This could be procedures not being followed, changes made without change request or a system and/or associated component malfunctions.
Immediate action
The Root Cause analysis of the Deviation in place can enable immediate action on how to stop the deviation and continue production. Using Corrective Actions afterwards will ensure that the deviation is properly closed. Preventive Actions will ensure that the deviation will not be reoccurring.
Process optimization
Your company will achieve immediate insight, as the modules are interlinked. The quick identification of the flow, from what led to the deviation to the corrective action gives you a complete overview and enables a smooth remediation process.
Modules in MyBlueLabel QMS Software
MyBlueLabel has a suite of modules to support the full ecosystem of processes to comply with regulations and international standards. The modules are integrated or can work as standalone modules.
