OneSC

Your One Source
of Truth.

OneSC connects supply-chain tracking, QA batch review, compliant e-signature, controlled documents and quality management in one ecosystem. Buy each product on its own. Integrate them when you are ready.

Back to Batch TrackerAwaiting Sign-off
Packaging Batch
PB 7781-02
Ibuprofen 400mg · NR000077 · Market UK
Bulk Batch
BB 5510-A
Quantity
10,000
Expected Arrival Date
26/07/2023
MA Holder
Nordic Pharma Ltd
QA Certification
Batch record reviewed21/07/2023 14:02
Deviations closed22/07/2023 09:18
Part 11 signaturePending
FDA 21 CFR Part 11 · EMA Annex 11 · GAMP 5Batch Right First TimeFive products · One record

The Ecosystem

Five products. One platform of record.

OneSC Platform

Full supply-chain tracking with QA batch review and certification. From PO to shipment, every batch visible and release-ready.

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OneLOGX

White-glove laboratory logistics for diagnostic samples with live tracking, environmental monitoring, and a complete digital chain of custody from collection to delivery.

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Coming Soon

OneESIGN

Dedicated 21 CFR Part 11 and EU Annex 11 electronic signature service, built for life sciences.

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Coming Soon

OneDOC

Template builder for controlled documents. Author once, reuse across batch records, SOPs and reports, creating a connected digital thread between documents, operators and production systems.

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Coming Soon

OnEQMS

Electronic quality management system. Deviations, CAPA and change control connected to the batches they affect.

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Standalone

Start with one product.

Own licence, own data model, own validation pack. Deploy the product that solves your most urgent problem and nothing else.

Integrated

Connect them when you're ready.

Connected to one another

Signatures, documents and quality events attach to the same batch record. One audit trail across the ecosystem, no middleware, no duplicate entry.

Interoperable with your systems

Works alongside the ERP, MES, LIMS and QMS you already run, exchanging data through open APIs.

Compliance

Compliance is the baseline, not a feature.

Designed and validated for regulated manufacturing from day one.

21 CFR Part 11Compliant electronic records and signatures.
EU Annex 11Computerised-system controls for GMP.
Full Audit TrailImmutable, time-stamped, attributable.
Human in the LoopSmart checks flag anomalies and late batches early. Qualified people make every release decision.
Validation PackIQ/OQ documentation with every release.
Data IntegrityALCOA+ principles enforced by design.

Proudly part of

See the ecosystem on your batches.

A 30-minute walkthrough with a OneSC product specialist.