Pharma & Biotech Contract Manufacturers

Every batch has to be able to defend itself.

Between batch records, training compliance, and an auditor who could show up any week, pharma and biotech contract manufacturing doesn't leave room for "I think so." BHIVES gives your floor a record that's built as the batch runs, not reconstructed for the binder afterward.

What running a regulated floor actually feels like

An auditor asks for the training record behind a specific batch, and someone has to go find it. A deviation gets logged after the fact, from memory, because the system was down or nobody had time. Capacity planning happens on a spreadsheet that's already out of date by the time the week starts. A customer wants status on their lot today, not after someone pulls the paperwork together.

It shows up as a documentation gap that turns a routine audit into a bad week, a qualified operator pulled onto a line they weren't trained on because the schedule didn't hold. They're Tuesday.

How BHIVES fits into that day

Every batch carries its electronic production record as it runs, tied to the operator, the equipment, and the training on file, so the audit trail already exists when someone asks for it. Training compliance is tracked against the work being assigned, not checked separately after the fact. Capacity planning adjusts to what's actually running, not a static plan. Quality events get caught and logged inside the workflow, not reconstructed afterward.

It's one batch, defensible from the start.

Built for regulated production

Pharma contract Manufacturing Workflow Automation, nutraceuticals, biotechnology manufacturing, medical devices, and life sciences operations all answer to the same bar: prove what happened, who did it, and that they were qualified to. BHIVES was built to carry that proof as a byproduct of running the floor, not a separate task.

Let's see your floor, not just ours

Tell us about your production, and we'll show you what BHIVES looks like running on it.