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. No credit card. Notes is free for 20 days.
30-minute demo. We'll show you how meeting signals become a plan that maintains itself.