Experiment Templates
Reusable, controlled templates that standardise experiment recording.
Experiment Templates give scientists a controlled starting point for every experiment type, pre-configuring the fields, calculations and required attachments so records are consistent from the first entry.
What Experiment Templates delivers
A controlled path from start to closure
- 1Design Template
- 2Review
- 3Approve
- 4Publish
- 5Use in Experiment
- 6Retire / Revise
Why teams move to Experiment Templates
Cut the time scientists spend formatting each new entry
Standardise how experiment types are recorded across teams
Reduce missing data through mandatory field enforcement
Keep template changes controlled and traceable
Make cross-experiment data comparable from the outset
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.