Industry: Pharmaceutical & Life Sciences
Chain of custody, GMP records, and serialization — continuously linked to the standards you operate under.
21 CFR Parts 210/211 (GMP), DSCSA serialization, FDA storage and chain-of-custody requirements, USP <797>/<800> for compounding. Structify Industrial maps your existing evidence to the regulations that govern it.
Systems we build on
Your stack, not a net-new platform.
SAP ECC / S/4HANA (QM, WM), Oracle, TraceLink, MasterControl, Veeva Vault, Dynamics 365
Where hours leak
Pharmaceutical & Life Sciences operators know the week. It looks the same every month.
Where hours leak today
- Chain of custody documentation requires manual assembly across receiving, storage, and distribution records.
- GS1/NDC reconciliation against the FDA database is time-consuming and error-prone at volume.
- FDA-compliant storage records span multiple systems and paper logs that are difficult to correlate.
- Pharmacist verification audit trails are reconstructed manually for each inspection cycle.
What Structify ships
- Chain of custody evidence linking from receipt through distribution
- GS1/NDC barcode reconciliation against FDA database
- Storage and environmental monitoring record correlation
- Pharmacist verification and cataloging audit trail automation
What we ship
Builds we deliver for pharmaceutical & life sciences shops, on the ERP you already run.
Connectors
Structify offers 3000+ Connectors
Salesforce, Google Drive, Email, Excel, and more — plus custom agents for mainframe and proprietary systems.
Scope it on your stack.
Bring one audit you're dreading. We'll wire it against your ERP and QMS and hand back a working version.