Solving the operational problems no one else wants to touch.

We don’t replace your systems, we fix what falls between them.

Pharmaceutical manufacturing is one of the most complex, compliance-driven industries in the world.

Behind every delay, deviation, or rework hour is the same root issue: planning doesn’t reflect how your plant actually runs. We solve the problems that spreadsheets, ERPs, MES and other platforms can't, the ones that cost you time, capacity, and trust.

About-img
See how

Why planning breaks in pharma

No matter the dosage form, every schedule is GMP-aware by design and delivers fast ROI:

Plans aren’t stable. They don’t hold beyond 24–48 hours.

People, equipment, and QA aren't aligned. Everyone works hard, but not together.

Constraints aren’t visible. Cleaning, QA, process timings, and material status are handled offline.

Teams plan in silos. Operations, planning, QA, and packaging use different tools and calendars.

When it breaks, it breaks big. A single shift change, bad operation sync, or QA hold derails the week and can lead to shortages.

About-img
See it in action

The problems we solve

These aren’t software problems, they’re production problems. Schedules don’t hold, teams aren’t aligned, and capacity is lost in ways no ERP or Excel file can detect. We built AIM | Pace to solve the real issues behind firefighting, missed OTIF targets, and unstable execution, the ones every pharma plant deals with, but few talk about openly.

Unstable schedules

"Our plan never holds more than 2 days"
Plans collapse within days, forcing constant rescheduling and firefighting.
Learn more ->

People & equipment out of sync

"QA’s not ready. We have to resterilize the cork bowl. The operator's on another shift."
Operators, rooms, and QA tasks aren’t aligned, causing idle time and missed windows.
Learn more ->

Reactive planning

"We can barely think ahead of the next shift."
Every change triggers a scramble, eating up planner time and eroding reliability.
Learn more ->

Unused (hidden) capacity

"We’re always full, but somehow still behind."
Usable cleanroom time, equipment slots, and operator hours go unnoticed and unused.
Learn more ->

GPM compliance bottlenecks

"We plan around cleaning manually, and hope it works."
Cleaning rules, hold times, and zoning are handled manually, slowing execution.
Learn more ->

Slow product ramp-up

"New products break the calendar, every time"
New SKUs or tech transfers disrupt calendars and take weeks to stabilize.
Learn more ->

Why partner with us

We don’t just provide solutions to your toughest problems, we build long lasting innovation partnerships.

Co-develop with your teams.
We work side-by-side with your planners, operators, and quality teams to shape features that address real-world bottlenecks and fit seamlessly into your workflows.

Applied Research Pipeline
We continuously turns frontline manufacturing challenges, from changeovers to lab release sync, into deployable features that evolve with your operations.

Built-In GMP & Pharmaceutical Expertise
Purpose-built for sterile injectables, OSD, biologics, and more. Every feature is designed for large-scale workflows with compliance at the core.

Do any of these sound familiar?

Let’s walk through what’s happening on your floor, and how we’d fix it.