Guides/Platform tour

Getting Started6:14

Platform tour

A guided tour of MoniDoseQMS after you log in — your profile, the everyday tools (notifications, recycle bin, tasks, events, regulatory news), and the dashboard.

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Once your QMS is set up and you log in, here's a tour of the everyday tools that keep your quality work organised — from your profile to the dashboard.

What the tour covers

1
Your profile & security
Manage your personal data and enable two-factor authentication. You can remove your account at any time.
2
Recycle bin
Deleted a document or record by accident? Restore it — items stay recoverable for 90 days before they're permanently removed.
3
Feedback & recent activity
Share feedback and see what's happening across your platform at a glance.
4
My tasks
Open tasks assigned to you across any module, jump straight to the record, and mark them complete — every action is date- and time-stamped.
5
Events
Create calendar events, tag the users who should take part, link an event to a specific module, and attach files or pick from the library.
6
Regulatory news
Stay up to date with the regulatory authorities that matter to you, browse the latest articles, and click through to the original source.
7
Dashboard
See what's open or overdue, your compliance health across document control, CAPA, training, risk, and audits, plus quality intelligence, training analysis, and CAPA aging.
8
User guide & validation guide
Built-in documentation for anything you want to understand in depth, plus the validation guide showing the platform is validated.

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Build your own QMS

Register an account and assemble your quality system from only the modules you need — set up in minutes, with no implementation fee.

Document Management Hub

A deep dive into the Document Management Hub — create controlled documents, link them across modules, route them through review and approval, sign with 21 CFR Part 11 e-signatures, and archive records for the long term, all inside MoniDoseQMS.

Change Control

Walk through MoniDoseQMS's change control module — create change requests, set priority and type, link to any QMS module, run impact assessments, attach documents, and manage the full review and approval workflow.

Deviations, CAPA & Preventive Actions

Walk through deviations, non-conformance reports, CAPA management, preventive actions, notes, and the records archive — the full corrective-and-preventive workflow inside MoniDoseQMS.

Risk Management

Walk through MoniDoseQMS's risk management module — create risk assessments based on ISO 14971, score probability and severity, apply control measures, and track residual risk with full traceability.

Design & Development

Walk through design projects and the full design control lifecycle in MoniDoseQMS — from design input and output to verification, validation, transfer, change control, and labeling, all aligned with FDA 21 CFR 820.30, EU MDR, ISO 13485, and IEC 62304.

SOP & ISO Template Library

Browse the built-in SOP and ISO template library in MoniDoseQMS — start from hundreds of pre-written, standards-aligned templates instead of a blank page, then customise and route them through document control.

Platform Overview

A complete walkthrough of MoniDoseQMS — see how the whole platform fits together, from building your quality system to running day-to-day quality work across all 13 categories.