Pharmaceutical Logistics for Research and Contract Labs
Research and contract labs move material for other people: samples for a sponsor, reagents between sites, investigational product for a study they are running on someone else's behalf. That means the record has to satisfy not just a regulator but the client, who may audit at any time. PharmaLogiks Enterprise gives a lab the custody, cold-chain, screening and signature records to answer any of them, on infrastructure the lab owns and controls.
The contract-lab problem
A lab that ships on behalf of clients carries the client's compliance risk as well as its own. Samples and investigational material need custody and temperature integrity from door to door. Sponsors expect accountability and clean documentation. Multiple clients mean multiple studies, references and cold-chain profiles running at once. And when a client audits, the answer has to be one clean export, not a scramble across a courier portal, an email thread and a spreadsheet.
How PharmaLogiks fits
Client-ready audit packs
The full record, custody, cold chain, screening, signatures and generated documents, exports as one inspection-ready bundle for any client audit.
Multi-programme by design
Divisions, scoping and per-programme references keep many clients and studies cleanly separated on one platform.
Custody and cold chain
Hash-chained custody and continuous temperature monitoring with early-warning projection on every shipment.
On your own infrastructure
Single-tenant and on-premise, so client and study data stays on the lab's own network, not a shared cloud.
See the full platform or how on-premise deployment works.
Common questions
Yes. PharmaLogiks assembles the complete record for a shipment, custody, cold chain, screening, signatures and generated documents, into one inspection-ready export, so a client or sponsor audit is answered from one place.
See it live in 25 minutes.
Eight guided flows: compliance review, DPS screening, Part 11 e-signature, custody chain, breach prediction, GDPR erasure and the validation report. Then a 90-day pilot on your own programme, fully creditable.