CARA LIMS. One system for your entire QC lab.

No more paper processes or disconnected point solutions. Manage your samples, execute test methods, track specifications, and review by exception, all in one place.Connected to your QMS, Batch Records, and Quality Documents without a single integration.

Your lab shouldn't run on numerous separate systems.

Compliance exposure

Paper records and manual transcription create audit findings. CARA LIMS enforces approved methods automatically every action captured, every result verified.

Batch release held up

Separate systems mean reconciling evidence before every release. CARA LIMS connects test execution, results, and review in one place, so release isn’t a wait.

Compounding costs

Per site, per instrument, per study, lab tools charge more as you grow. CARA LIMS runs on a single user licence across your entire QC estate.

Governed record types. No boundaries to cross.

Every sample, test, result, method, instrument, reagent, investigation, specification, and stability record shares the same audit trail.When something goes wrong, the evidence is already linked, not scattered across systems waiting to be assembled.

Licensed per user not per site, instrument, or study.

How every sample moves through the system

01

Register

Sample raised against a specification. Chain of custody from sampling point.

Attributable

02

Test

Scheduled from the specification. Method version and instrument recorded.

Original

03

Result

Values evaluated against limits. Mandatory second-person verification.

Accurate

04

Review

Peer review then supervisor sign-off. OOS flagged; compliant results fast-track.

Verified

05

Disposition

QA releases, quarantines, or returns for retest. A state, not a field.

Enduring

Every step enforced by lifecycle state. No step can be skipped. No result approved before it’s reviewed. Compliance by configuration, not by people remembering.

The lab joins the rest of the business

Every other LIMS stops at the lab door. CARA LIMS doesn't.

MODULE

CARA LIMS

9 governed record types · same licence · same audit trail

● CONNECTED TODAY

Quality

· QMS: CAPAs link directly to result records
· Controlled documents: same version control
· Batch records: no reconciliation before release
· Audit trail: one record, not six systems

Regulatory / RIM

Specifications in submissions = specifications in the lab. Same record, not a copy.

Clinical

Sample and result records referenced directly, no re-entry before submission.

Safety

PSUR drafting can draw from live governed lab data, not exported snapshots

Same licence. Same users. Same audit trail. The rest of the business is already waiting.

GET STARTED

Whether you're evaluating CARA LIMS for the first time or looking to add it to an existing deployment the conversation starts the same way.

No pricing commitments in the first conversation. We'll map it to your estate.