eQMS for regulated manufacturing
Replacing MasterControl – with Power IMS in Microsoft Teams
MasterControl publicly describes itself as an eQMS for regulated manufacturers (FDA 21 CFR Part 11, EU GMP Annex 11, ISO 13485, GxP) with document control, automated training management, CAPA, audits and no-code form designer.
7 comparison points
6 of 7 points covered
7 editorial comparison points; not a measurement of complete feature parity. 7 vendor claims not yet verified in detail.
Mapped Power IMS capabilities
Document control & versioning
Document control with status, metadata, versions and approval workflow in Teams; stored in your tenant's SharePoint.
Training & read receipts
Read receipts in Power QMS; training, competencies and acknowledgement matrix in Power Knowledge.
Nonconformities, CAPA & complaints
Findings, deviations and corrective actions from audits in Power Audit; improvement actions and complaint handling via Power CI with assessment and implementation tracking.
Audits & actions
Audit programme, checklists, findings and action tracking in Power Audit.
No-code forms
Custom forms without programming via the form builder in Power QMS.
Permissions, search & notifications
Uses Entra ID, SharePoint permissions, Microsoft Search and Teams notifications – no separate user management.
Capability comparison: MasterControl and Power IMS
| Area | MasterControl (per vendor) | Power IMS as replacement |
|---|---|---|
| Document control & versioning | Document control with immutable, audit-ready records. Not yet verified in detail – no claim that features are absent | Matching module Document control with status, metadata, versions and approval workflow in Teams; stored in your tenant's SharePoint. |
| Training & read receipts | Training and exams start automatically from changes, CAPA and production records. Not yet verified in detail – no claim that features are absent | Matching module Read receipts in Power QMS; training, competencies and acknowledgement matrix in Power Knowledge. |
| Nonconformities, CAPA & complaints | CAPA linked to audit findings. Not yet verified in detail – no claim that features are absent | Matching module Findings, deviations and corrective actions from audits in Power Audit; improvement actions and complaint handling via Power CI with assessment and implementation tracking. Scope / open: CAPA and complaints are confirmed via Power Audit and Power CI; identical root cause analysis, escalation and effectiveness verification need workflow-level verification. |
| Audits & actions | Audit findings linked to corrective actions. Not yet verified in detail – no claim that features are absent | Matching module Audit programme, checklists, findings and action tracking in Power Audit. |
| No-code forms | Own forms and workflows via no-code designer. Not yet verified in detail – no claim that features are absent | Matching module Custom forms without programming via the form builder in Power QMS. |
| Regulated industries & e-signatures | FDA 21 CFR Part 11, EU GMP Annex 11, ISO 13485, GxP. Not yet verified in detail – no claim that features are absent | Individual review No FDA 21 CFR Part 11 / EU GMP Annex 11 validation claimed – assess individually for GxP and medical-device requirements. |
| Permissions, search & notifications | The application's own user, permission and notification management. Not yet verified in detail – no claim that features are absent | Via Microsoft 365 Uses Entra ID, SharePoint permissions, Microsoft Search and Teams notifications – no separate user management. |
Power IMS fits if …
You are an SME without FDA/GxP obligations and want a management system in Teams.
MasterControl remains sensible if …
You are subject to FDA/GxP and need validated electronic signatures.
Vendor information summarised from publicly available sources as of 4 November 2026. No rating or testing of the third-party system; your edition and configuration may differ. Please let us know about any inaccuracies.
What remains individual – and how we handle it
We clarify these points in the replacement check before you decide.
Regulated industries & e-signatures
No FDA 21 CFR Part 11 / EU GMP Annex 11 validation claimed – assess individually for GxP and medical-device requirements.
Five steps from MasterControl to Power IMS
- 1
Replacement check
Together we capture how you use MasterControl today: modules, document types, workflows, integrations and obligations.
- 2
Target picture & trial
You test the matching Power IMS modules in Teams with your own examples before deciding.
- 3
Setup
Install the Teams apps and set up SharePoint storage, roles and approval workflows via the setup portal.
- 4
Content & migration
Transfer documents, processes and lists; clarify export options, histories and retention duties beforehand.
- 5
Go-live & retire the old system
Training, a parallel phase if needed, then cancelling MasterControl in line with your contract term.
Better fit: Power IMS or MasterControl?
Power IMS fits if …
You are an SME without FDA/GxP obligations and want a management system in Teams.
MasterControl fits if …
You are subject to FDA/GxP and need validated electronic signatures.
FAQ on replacing MasterControl
What happens to our content from MasterControl?
Documents and lists are transferred to your SharePoint. Which metadata, versions and histories can be exported depends on the old system and your contract and is clarified in the replacement check.
Do we need to run both systems in parallel?
Not necessarily. A short parallel phase can make sense until audits or approval cycles are completed.
How long does the replacement take?
Power IMS is ready to use as a standard Teams app. The duration depends mainly on the scope and quality of the content to transfer.
Where is our data stored afterwards?
In the SharePoint of your own Microsoft 365 tenant; permissions use your existing Microsoft 365 accounts.
Replacement check for MasterControl
In a short meeting we review your usage and show the matching modules live in Teams.
MasterControl, Microsoft, Teams and SharePoint are trademarks of their owners, used for identification only; no affiliation with these vendors. Based on public vendor sources, without warranty; does not replace technical or legal review. Information inaccurate? Contact info@powermanufaktur.com and we will correct it promptly.
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