Sample Management
Registration, scheduling, allocation and status control for every sample.
Sample Management is the entry point of the laboratory workflow, capturing sample identity, source, specification and required tests at login and tracking status through every subsequent stage.
What Sample Management delivers
A controlled path from start to closure
- 1Login
- 2Specification Check
- 3Test Plan Assignment
- 4Queue
- 5Status Update
- 6Disposal
Why teams move to Sample Management
Eliminate paper logbooks for sample intake
See every sample's status without asking the lab
Cut turnaround time with automated test assignment
Prevent unspecified or duplicate sample entries
Simplify retention sample recall for investigations
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.