Document Templates
Standardised templates that enforce format and required content.
Document Templates enforce a consistent format and mandatory content structure for every document type, so authors start from an approved layout rather than a blank page.
What Document Templates delivers
A controlled path from start to closure
- 1Design Template
- 2Review
- 3Approve
- 4Publish
- 5Author from Template
- 6Retire / Revise
Why teams move to Document Templates
Standardise format and structure across every document type
Cut authoring time with a pre-approved starting point
Reduce formatting errors caught late in review
Keep template changes controlled and version tracked
Give new authors built-in guidance at the point of writing
Built for regulated operations
21 CFR Part 11
Electronic records and electronic signature controls — unique user identity, secure e-signatures and computer-generated audit trails on every record.
EU GMP Annex 11
Computerised system controls including access management, change control, data integrity and periodic review of the system.
GAMP 5
Risk-based validation approach, with pre-executed IQ/OQ documentation supplied with every release.
ALCOA++
Records that are attributable, legible, contemporaneous, original and accurate — enforced at record level.
OPS IQ is designed to support these regulatory expectations. Compliance is achieved together with your own validated implementation, procedures and controls.
Connected to your enterprise systems
ERP / SAP
Master data, materials and batch context exchanged over open REST and event APIs.
MES
Shopfloor execution events and equipment context linked to quality records.
LIMS
Laboratory results and specification data connected to quality decisions.
Identity Providers
Enterprise SSO and role-based access through your existing identity provider.
Enterprise APIs
Open REST and event APIs for custom and legacy systems.