Pharmaceutical LIMS built for QC release, not a generic sample tracker
Bind every result to the method version, the analyst, the instrument calibration, and an electronic signature your quality unit can defend.
- 21 CFR Part 11
- EU Annex 11
- GxP
- ALCOA+
- ICH Q7
What these labs track in LabPi
Sample types and work products for this lab, not a generic tube list.
- Raw materials
- In-process samples
- Finished product
- Stability pulls
- Packaging
- Environmental monitoring
How the work actually runs
Specification-bound testing
Each lot inherits the approved spec, tests, and limits. Analysts cannot skip a required step without a documented deviation.
Review and batch release
Results move through analyst and QA sign-off. The electronic batch record keeps materials, instruments, and signatures together.
Deviation to CAPA
Out-of-specification and out-of-trend events open a linked deviation, with root cause and effectiveness checks still attached to the lot.
LabPi capabilities this lab uses
Each card opens the product page for that capability, so you can see the feature behind the industry claim.
21 CFR Part 11 and e-signatures
Meaning of signature, authority checks, and a non-repudiable audit trail.
View capabilityElectronic batch records
Digital batch sheets with genealogy, in-process checks, and PDF export.
View capabilitySOP enforcement
Version-locked methods so the bench runs the approved procedure, not last month’s copy.
View capabilityEquipment calibration lockout
Out-of-calibration instruments cannot be used to generate releasable results.
View capabilityRelated labs
See LabPi on a pharmaceutical workflow
A 30-minute demo uses your sample types, your reports, and the regulations on this page.