Keep the work moving. Keep the record straight.
DLBD gives quality, laboratory, manufacturing, warehouse, and R&D teams software that fits the way they work—with shared controls wherever the work connects.
Throughput · 14 days
samples/dayResult outcomes
Built to adapt to your regulatory regime: 21 CFR Part 11 · ISO 17025 · ISO 13485 · ISO 9001 · GxP
How we run compliance →The controls belong in the system, not on your team’s shoulders.
Regulated teams have spent too long choosing between oversized enterprise software and a patchwork of spreadsheets, documents, and point tools. DLBD replaces that tradeoff with applications that are easy to work in, difficult to misuse, and ready to connect when the work crosses departments.
Start anywhere. Everything connects.
Vapor runs the lab. Fluid runs quality. Batch records, warehouse, and ELN cover the work around them. Use one on its own, or bring them together without rebuilding the same users, records, and controls in every system.
From first observation to signed result.
Keep quality moving and the evidence close behind.
Batches and stock that account for themselves.
Shared controls, identity, and traceability.
Fewer clicks between sample and answer.
Give the bench back its time. Vapor removes the menu-diving, repeat entry, and password interruptions that turn routine result work into an all-day task.
- 1Scan a sampleOne barcode scan, no menu-diving with gloved hands.
- 2Scan-and-prepVapor returns the sample and every pending test in a single call.
- 3Enter every result at onceAtomic bulk entry: all-or-nothing, no half-saved batches.
- 4Two-person verifyA verifier who is not the creator signs. The record locks.
- 5Certificate issuedA branded, versioned Certificate of Analysis, generated.
Every change, attributed and immutable.
Stop rebuilding the story after the fact. Every change carries its own history, so questions are answered in minutes and audit prep stops consuming the week.
Audit trail · Result R-8842
- 1Open any recordEvery record that matters carries a history that cannot be edited after the fact.
- 2Who, what, whenEach change is attributed and time-stamped for you, with nothing to log by hand.
- 3The reason, on the recordThe §11.10(e) context an auditor asks for is already written before anyone asks.
See the problem while there is still time to act.
Aging CAPAs, slipping turnaround, expiring training, and drifting throughput surface where the work happens—not three weeks later in a month-end spreadsheet.
Turnaround trend
Volume by category
CAPA aging
days openEvents by type
Start with one product. Add the next when it earns it.
Every DLBD product stands on its own, and none of them forces you into the rest. Add another later and it switches on beside what you already run: same login, same audit trail, nothing to re-enter and no migration to dread.
What usability-first compliance buys you.
Take the work for a spin.
Follow a sample, close a CAPA, and see how the records stay connected. The demo is live in your browser.