Instrument Integration
Direct acquisition from analytical instruments and chromatography systems.
Instrument Integration connects HPLC, GC, dissolution systems, balances and chromatography data systems directly to the lab record, removing manual transcription and the errors it introduces.
What Instrument Integration delivers
A controlled path from start to closure
- 1Dispatch Method
- 2Acquire Result
- 3Map to Sample
- 4Validate
- 5Store Raw Data
- 6Release to Review
Why teams move to Instrument Integration
Remove manual transcription as a source of lab error
Speed up result entry from instrument to record
Retain raw instrument data for every reported result
Reduce out-of-specification events caused by keying errors
Support data integrity with a direct instrument-to-record chain
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.