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Structure sensitive collaboration without slowing critical work.

Turn every clinical trial, care initiative, and compliance workflow into a governed Microsoft 365 workspace — evidence in, audit trail out.

The repeatable work.

Providers: service-line initiatives, care-pathway redesigns, incident response, patient-journey projects.

Pharma / biotech: clinical trials by site, CRO collaboration, medical affairs and MSL engagement.

The lifecycle.

Providers: Intake → coordination → treatment plan → discharge → follow-up.

Pharma: Protocol → site activation → conduct → close-out → analysis.

Where collaboration leaks.

The work is cross-functional, regulated, document-heavy, and time-sensitive. Clinical trial site workspaces (sponsor ↔ CRO ↔ investigator) are rebuilt from scratch per study — protocol amendments, SAE reporting, and site documentation pile into email. Hospital service-line initiatives run as ad-hoc task forces with no persistent workspace — knowledge dies at project end. Medical affairs and MSL teams lack structured workspaces for HCP engagement and KOL planning, creating compliance exposure every time.

What nBold changes.

Ready-to-work templates for every clinical, operational, and medical-affairs motion.

A trial site workspace per protocol. A service-line project workspace per initiative. A medical affairs engagement workspace per programme. Each one starts with documents, tasks, intake forms, and governance already in place.

Context that carries across the patient and trial lifecycle.

Intake → coordination → discharge → follow-up stays connected. Site activation → conduct → close-out is one traceable lineage. Handoffs stop losing context.

Compliance built in, not bolted on.

Sensitivity labels, membership rules, and audit trails apply automatically. ISO 27001 certified. SOC 2 Type II certified. Inspection-ready by default.

Every trial, every service-line initiative, every care pathway starts with the right workspace — and context moves with the work, not against it.

Proof points.

ISO 27001 certified · SOC 2 Type II certified · Microsoft 365 native · Sensitivity labels · Audit trail · Lifecycle management for closed trials.

$2.3B
Average cost to develop a new drug; trial complexity is the largest driver of cycle-time extension.
Deloitte, 2025 Global Life Sciences Outlook
20–30%
Top-quartile pharma ops deliver trials 20–30% faster through standardised cross-functional workspaces.
McKinsey, Digital Transformation in Pharma 2024

Repeatable collaboration for the care you deliver.