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Applied AI for large-scale drug manufacturing

AIM | Pace™

Coordinating changeovers, release timings, shared resources, and shifting priorities challenges even the best-run plants.

AIM | Pace turns that complexity into GMP-compliant daily and weekly production plans that adapt in real time to shop-floor realities.

Built for sterile injectables, OSD, biologics, non-sterile liquids, suspensions, creams, and more, it delivers stable operations, higher throughput, and reduced overtime, all without added CapEx.

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Features and Capabilities

Our AI-powered planning platform improves the efficiency of your cleanroom assets with:

Adaptive, granular scheduling for large-scale drug manufacturing

Plans and aligns every step, changeovers, campaign sequencing, line availability, cleaning, tool prep, and labor, into one unified schedule that meets delivery targets while staying fully GMP-compliant.

Optimized Resource Utilization & Real-Time Adjustments.

Maximizes the use of critical production assets, from tablet presses and coating lines to utilities, packaging stations, and skilled labor, while dynamically adjusting plans to prevent bottlenecks, minimize idle time, and keep batches moving.

Instant Priority Adjustments for Faster Decision-Making

Give supervisors full control to rapidly adapt production when priorities shift, rescheduling tasks, reallocating equipment, and preventing costly downtime in real time.

Regulatory-aware engine

All scheduling decisions are automatically bounded by GMP and site-specific compliance rules, ensuring every plan, adjustment, and resource allocation meets regulatory standards while remaining audit-ready.

Fast, Seamless Integrations

Connects effortlessly with your ERP, MES, SCM, and lab systems, preserving your existing processes instead of forcing you to change them. Our lightweight approach delivers reliable data integrity and fast go-live without disrupting daily operations.

Changeover & campaign optimization

Plans complex routings and intelligently sequences changeovers to minimize downtime between products or batches. Supports multi-SKU, multi-line operations across all dosage forms, improving throughput while maintaining cleaning and validation compliance.

Energy usage optimization

Schedules production and equipment usage to lower peak energy demand and reduce idle runs, cutting costs and GHG emissions while supporting ESG and sustainability goals, without sacrificing your throughput or quality.

Lab & QA Release sync

Coordinates lab testing, QA approvals, and production schedules so batches move seamlessly through release gates. Reduces waiting time between departments and helps keep delivery timelines predictable under strict GMP controls.

Innovation at it's core

Driven by an applied research pipeline, AIM | Pace evolves with your plant’s challenges, rapidly turning frontline problems like routing conflicts, lab bottlenecks, or energy inefficiencies into deployable AI features that keep you ahead of operational demands.

Turning complexity into capacity.

AIM | Pace delivers very fast ROI and operational stability across diverse pharma sites, unlocking capacity and improving flow without major capital investment.

+10% Capacity gain

Achieved by uncovering hidden throughput potential on existing lines, no added shifts or CapEx, just by purely optimizing production sequencing and timings.

Fewer firefighting shifts

Stable, conflict-free schedules reduce last-minute rescheduling and weekend overtime.

Improved planning productivity

Less manual Excel work means more focus on decision-making, not spreadsheet versioning.

+20% More efficient workflows

Validated at one of Canada’s largest sterile injectable plants through smarter sequencing and fewer idle periods.

Shorter batch release delays

Better lab & QA synchronization cuts idle time between departments.

Confidence in every decision

Traceable, compliant scheduling reduces errors and eliminates the scramble before inspections.

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.

Discover our story

Freaquently Asked Questions

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1. Can Kaster be integrated with my ERP?

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Service Provided As: The Service is provided for free during this pilot project, and is provided “as is” with no warranty. Conclude will provide User support for the Service, however; Conclude is not committed to any level of service or availability of the Service. A further description of the Service and our user support is available at the Site.

Company Liability: The Service is provided for free during this pilot project, and is provided “as is” with no warranty. Conclude will provide User support for the Service, however; Conclude is not committed to any level of service or availability of the Service.

2. Is Kaster subject to GxP regulations?

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3. How long is the integration and deployment phase?

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4. I have another use case in mind, can Kaster help?

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5. Can I cancel anytime?

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7. Can I use Kaster on all my devices?

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8. I already have an APS software, will Kaster replace it?

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9. Is Kaster available outside of Canada?

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10. Does Kaster allow for manual schedule adjustments?

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11. How long does it take to produce an optimized production plan?

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See it in action

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