AI for CDMOs
Governed AI, built around the process you already run.

Build reusable quality workflows around the process you run, while making client-specific evidence, approval and deployment requirements explicit.

Talk to UsExplore Your Challenges
BUILT AROUND YOUR WORK

A consistent process. The right context for each client.

Client programmes bring different procedures and obligations. Useful AI needs to fit those boundaries as well as the operational workflow.

CDMOsIllustrative workflow · explore a challenge
WHERE THE WORK GETS STUCK

A quality event needs the right client context and approvers, rather than a generic investigation route.

Programme quality event
Client procedure & approval matrix
WHAT YOUR TEAM GETSFor human review

A programme-specific case review

  • Programme context attached
  • Required reviewers identified
  • Approval route defined
DECISION OWNERProgramme quality lead
HOW WE HELP

Configure the case fields, evidence requirements and approval gates around the programme's agreed process.

Explore the relevant workflowsCAPAChange Control
Deployment optionsDedicated

Run in a dedicated in-country environment, or entirely inside your infrastructure.

Explore the foundation
WHAT WE BRING TO THE TABLE

AI in contract manufacturing: the modules that matter most.

We scope the combination around your process and data. Each workflow below has its current development status shown.

01Most developed workflow
Quality & Manufacturing

CAPA

Investigations that hold up.

Coaches your investigators with comparable cases and root-cause checks. Only your people can approve or sign.

Explore CAPA
02Supported workflow
Quality & Manufacturing

Change Control

Know what a change triggers.

See comparable past changes and the validation work this one may trigger. A named person decides.

Explore Change Control
03Supported workflow
Quality & Manufacturing

AMV

Method history, in reach.

Method history retrieved and documentation drafted — judgement and approval stay with your scientists.

Explore AMV
More workflows for CDMOs3 more
THE OUTCOME TO DESIGN FOR
  • A workflow built around your existing process
  • Organisational knowledge, prepared and retrievable
  • A deployment matched to your data and regulatory obligations
A PRACTICAL FIRST CONVERSATION

Start with one programme and its agreed operating boundaries.

You do not need a finished specification. Start with the work you want to improve.

01 / YOUR CONTEXT

What helps us understand the problem

  • A programme workflow to improve
  • Its review and approval requirements
  • Client data and deployment constraints
02 / OUR DISCUSSION

What we’ll work through together

  • What can be standardised across programmes
  • What needs programme-specific configuration
  • Where the system should run and who can access it
Bring the people closest to the work
Head of IT or Digital TransformationHead of QualityValidation leadership

Build around the process you already run.

Let’s map one programme’s workflow, client obligations and deployment needs before deciding what to build.

Bring your challenge.
Let’s find the right next step.

Talk Through Your Challenge
Looking at a different type of organisation?
Pharmaceutical ManufacturersGeneric ManufacturersBiotech & DiscoveryResearch Teams

Leave your details and someone from the team will be in touch.

Interested inPick one or more

We'll only use this to reply about your enquiry.