This walkthrough focuses on project isolation, document generation, and audit-ready traceability for multi-client work.
Jump between client workspaces, review version history, generate GMP docs, and open audit trails fast.
These are the operational gaps that usually show up first.
Juggling formulas across dozens of clients in shared folders and spreadsheets leads to mix-ups, version confusion, and costly errors that erode client trust.
Manually compiling Manufacturing Formula Records, Batch Production Records, and specifications burns 15-20 hours per week that your chemists should spend formulating.
When an auditor walks in, scrambling to locate batch records, change histories, and traceability docs across multiple systems is stressful and risky.
Without proper separation, one client's proprietary formulas are just a wrong click away from another client's view. Confidentiality is a constant liability.
Purpose-built tools that fit the way you work.
Every client gets a dedicated workspace with its own formulas, raw materials, batches, and team permissions. Zero cross-contamination of proprietary data.
Generate Manufacturing Formula Records, Batch Production Records, and product specifications instantly. Every document follows GMP formatting standards out of the box.
Cryptographic audit trails track every change. Pull complete traceability reports in seconds, not days. Walk into any audit with confidence.
Assign chemists, QA reviewers, and production staff to specific client projects with granular permissions. Everyone sees exactly what they need and nothing more.
Row-level security enforced at the database layer means one client can never read another’s raw materials, formulas, or batch records — even through the same Formuley account. Formuley employees cannot see your client formulas. We make money from your subscription, not from their IP.
Full security overviewOnboard as many clients as you need. Each workspace is fully isolated with independent formulas, raw materials, and batch records.
Auto-generate MFRs, BPRs, and CoAs that meet FDA 21 CFR Part 211, EU GMP Annex 15, and ISO 22716 requirements.
One-click compliance reports with hash-chain verification. Every modification is timestamped, attributed, and immutable.
Define custom roles for chemists, QA, production, and client reviewers with fine-grained permissions per workspace.
Trace any finished product back to raw material lot numbers, supplier certificates, and production records in seconds.
Built-in compliance checks for FDA, EU, UK, Health Canada, Australia, Japan, and ASEAN regulatory frameworks.
Full formula versioning with branching, comparison, and multi-stage approval workflows for QA sign-off.
Dedicated support channel with 4-hour response SLA. Your lab doesn't stop, and neither do we.
Lab includes one premium public site with lab-mode sections for capabilities, trust signals, and quote-oriented calls to action.
Formuley is built to reduce the handoff friction between formulation, QA, production, and client review by keeping GMP records, version history, and traceability in one system.
Isolated
Client workspaces
One click
GMP docs
Versioned
Audit history
Batch to lot
Traceability
