Regulated industries
Food, pharma, cosmetics, and other GMP-adjacent environments where the record matters as much as the product. Audits, signatures, and traceability are non-negotiable, and paper is the bottleneck. Frontlink digitises execution while producing the evidence trail regulators expect.
What defines this environment
Audit-ready by default
Every action needs who, what, and when. Reconstructing events from paper takes days per audit.
Signatures and approvals
Critical steps demand review and sign-off, with roles and timestamps, in line with 21 CFR Part 11 and EU Annex 11 expectations.
Deviation and CAPA discipline
Non-conformances must be captured, classified, and closed with evidence.
Full traceability obligations
Recall readiness means lot-level genealogy across warehouse and production, provable in minutes.
Where Frontlink makes the difference
Quality checks with e-signatures
In-process checks with digital signatures and approval gates on the steps that require them.
Digital batch records and SOPs
Executed procedures and batch documentation are produced during the run, complete and legible.
Recall-speed genealogy
Trace any lot up and down in minutes, including warehouse movements and expiry status.
Timestamped event history
Machine states, operator actions, and quality events recorded with timestamps for a defensible audit trail.
Problems we solve in this environment
Each problem links to a deep dive: who feels it, why ERP alone doesn't fix it, and how Frontlink does.
Quality checks are on paper and defect data is scattered
Checks happen, but the data lives in binders and spreadsheets. Issues repeat because there's no structured trend analysis.
Compliance-grade audit trails and e-signoffs are missing
You can't prove who did what, when, and under which procedure version. Shared logins and wet signatures are the norm.
Nonconformances and corrective actions fall through the cracks
Issues are spotted but corrective actions aren't tracked. The same problems come back quarter after quarter.
Manual batch review causes release delays
Batch paperwork slows release. Missing signatures and incomplete forms create rework that adds days to the release cycle.
Operator work instructions are uncontrolled
SOPs exist in binders, but people don't follow the same steps every time. Version control is nonexistent.
Batch and lot traceability has gaps in internal genealogy
You can trace one step back and one step forward, but internal transformations (mixing, splitting, rework) are painful to reconstruct.
See it on your own lines
Join the waitlist and walk through your machines, your constraints, and what going live in weeks looks like.