zixov.pharma tech
All modules
DMS

Document Management

Controlled documents from draft to obsolescence

Author, review, approve, issue, and retire SOPs and controlled documents with a fully audit-trailed lifecycle. Version control, controlled copy distribution, and periodic review are built in.

21 CFR Part 11 EU Annex 11 ICH Q10 WHO GMP ALCOA+

Overview

Why document management matters

Your quality system runs on documents — SOPs, work instructions, specifications, policies, and forms. When those documents live in shared drives, email threads, and paper binders, every revision becomes a project and every audit becomes a scramble. Zixov Document Management replaces that patchwork with a single controlled repository where every document has one current effective version, one owner, and one complete history.

The module manages the entire lifecycle: structured authoring, routed review and approval, controlled release with effective dating, distribution of controlled copies, scheduled periodic review, and formal obsolescence. Because it shares a platform with Training, Change Control, and the rest of the suite, a document revision automatically triggers the downstream actions your procedures require — retraining, change assessment, controlled copy retrieval — without anyone chasing a checklist.

Everything is attributable and permanent. Every view, edit, sign-off, print, and retrieval is written to an immutable audit trail, so you can show an inspector not just the current SOP, but exactly how it got there.

70%

faster document approval cycles

100%

of documents within periodic review window

0

uncontrolled copies in circulation

Typical outcomes reported by teams moving from paper and spreadsheet-based processes to Zixov.

See it in action

Document Management inside Zixov

A look at the actual screens your team will work in — pick a view or let the tour play through.

app.zixov.com/documents

Document register

Site: Ahmedabad — Unit 1 · 1,284 effective

Granulation — line 2 cleaning

SOP-100234 · v4.0

QA approval

Due today

Sampling of raw materials

SOP-100198 · v4.0

Effective

01 Aug 2026

Purified water loop operation

SOP-100121 · v6.1

Effective

12 Jun 2026

Equipment logbook practices

SOP-100087 · v3.0

Periodic review

Due in 14d

Tablet compression setup

SOP-100305 · v1.0

Draft

A. Shah

One controlled register — every document with one effective version, one owner, one status.

Challenges we solve

The problems this module was built to fix

Uncontrolled versions in circulation

Outdated SOPs on desktops and shop-floor binders are one of the most cited audit findings. Controlled copy issuance and retrieval tracking ensure only the effective version is ever in use.

Slow, opaque approval cycles

Documents stuck in email review for weeks with no visibility. Routed workflows show exactly who has the document, how long they've had it, and escalate automatically on delay.

Missed periodic reviews

Biennial review dates tracked in spreadsheets get missed. Scheduled review cycles with reminders and escalations keep every document within its review window.

Audit preparation takes weeks

Reconstructing a document's history from paper records is slow and error-prone. A complete, immutable audit trail makes any document's full lifecycle retrievable in seconds.

Capabilities in depth

What DMS does, in detail

01

Structured authoring & templates

Create documents from controlled templates so every SOP follows your house style and required sections — no formatting drift, no missing headers.

  • Document-type templates with mandated sections and numbering
  • Draft workspaces with collaborative commenting
  • Automatic document numbering per your naming convention
02

Review, approval & e-signatures

Route documents through multi-stage review and approval with role-based sign-offs designed for 21 CFR Part 11 compliance.

  • Sequential and parallel review routing with due dates
  • Meaning-of-signature capture on every approval
  • Automatic escalation and delegation for absent approvers
03

Controlled release & distribution

Release approved documents with effective dating, issue controlled copies to specific locations, and track every copy to retrieval.

  • Effective dating with training-gate enforcement before go-live
  • Controlled copy issuance with numbered print tracking
  • Retrieval and destruction records on supersession
04

Lifecycle governance

Keep the document estate healthy with automated versioning, periodic review, and formal obsolescence — nothing lingers past its shelf life.

  • Automatic major/minor versioning with change summaries
  • Periodic review scheduling with reminder escalation
  • Controlled obsolescence with archival retention

How it works

The document management lifecycle in Zixov

1

Author

Create or revise a document from a controlled template, with drafts kept separate from the effective version.

2

Review & approve

Route through your defined review and approval chain with e-sign-offs and automatic escalations.

3

Train & release

Affected staff are trained on the new version before it goes effective on its scheduled date.

4

Distribute

Issue controlled copies where paper is required; electronic access always resolves to the current version.

5

Review & retire

Periodic review keeps content current; superseded and obsolete versions are archived with full history.

At a glance

Everything included

SOP authoring with structured templates and doc-control workflow

Multi-stage review and approval with e-signature-ready sign-offs

Controlled copy issuance, distribution, and retrieval tracking

Automatic versioning, effective dating, and obsolescence

Periodic review scheduling with escalation reminders

Complete, immutable audit trail on every document action

FAQ

Common questions about document management

Can we migrate our existing SOPs into Zixov?

Yes. Bulk import brings in your current effective documents with metadata (document number, version, effective date, owner) preserved, so you go live with your full document estate under control from day one.

How does the module handle paper on the shop floor?

Where paper is still required, controlled copies are issued as numbered prints tied to a location. When a document is superseded, the system generates retrieval tasks so every outstanding copy is pulled and its destruction recorded.

Are the electronic signatures compliant?

Sign-offs capture the signer's identity, date-time, and meaning of signature, backed by unique credentials and a full audit trail — designed to meet 21 CFR Part 11 and EU Annex 11 expectations. Your validation package documents the controls.

What happens when an SOP changes?

The revision can be linked to a change control record, and affected employees are automatically assigned retraining through the Training module. The new version won't go effective until your configured training gate is satisfied.

Better together

Works together with

Document Management is one part of a connected quality suite — records flow between modules automatically, so nothing is re-entered and nothing falls through.

See Document Management in a live demo

30 minutes, tailored to your workflows — bring one of your own processes and watch it run in Zixov.