Industry
Pharma
Pharma programmes span years and functions — clinical, regulatory, medical, commercial — where a dropped decision is expensive and traceability is non-negotiable. In Parallel was built for that.
Traceability is the default
Every decision and status In Parallel records traces back to the meeting and moment behind it. In a domain where you must show how a conclusion was reached, evidence-backed by design is the point.
Hold the programme together
Launches and trials coordinate across many teams running in parallel. In Parallel keeps one shared record across them, surfaces cross-functional dependencies, and detects drift before a milestone slips.
EU-hosted, governed
In Parallel is built and hosted in the EU, with workspace-scoped access and no model training on your data — the controls regulated programmes require.
FAQ
Common questions
- Is In Parallel suitable for regulated pharma programmes?
- Yes — it is EU-hosted, workspace-scoped, and never trains on your data, and every decision and status traces back to the meeting behind it for full traceability.
- How does it help long, cross-functional programmes?
- It keeps one shared record across clinical, regulatory, medical, and commercial teams, surfaces cross-functional dependencies, and detects drift before a milestone slips.
- Where is data stored?
- In the EU by default, with permission-scoped access and no model training on customer data.
Start with your next meeting.
Bring your team in. Use every surface, including every other team's. From €29 per user per month, billed monthly, no commitment.
30-minute demo. We'll show you how meeting signals become a plan that maintains itself.