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Platform

Platform overview System exchange AI and automation Compliance evidence Security and trust

Products

CTMS eTMF Suite map

For teams

Clinical teams Organizations Sponsors CROs Sites Biotech Academic and nonprofit
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Organizations

Built for the teams that carry the trial.

Sponsors, CROs, sites, biotech teams, and academic research groups share the same study reality. Clinistack gives each group the control surface that matches its work without fragmenting the record.

Discuss organization fit View clinical teams

Teams

The same study creates different work.

One study can mean Sponsor oversight, CRO delivery, site workload, lean biotech control, or academic research operations. The record stays coherent while the work surface changes.

Sponsors

Sponsor oversight, CRO accountability, amendment impact, safety context, vendor evidence, and inspection readiness.

CROs

Repeatable delivery, Sponsor-specific requirements, country variation, monitoring follow-up, RBM work, and client-visible evidence.

Sites

Coordinator queues, DOA and training currency, consent-version context, eISF/eTMF exchange, source evidence, and monitor follow-up.

Biotech

Lean Sponsor control, CRO-heavy trial oversight, vendor stack visibility, safety awareness, and a model that survives pivotal scale.

Academic and nonprofit

IRB cadence, EHR/source realities, grant constraints, coordinator turnover, and multi-study PI accountability.

Shared record

Different teams. Same controlled record.

Each page speaks to a different operator, but they all map back to the same trial context, record ownership, controlled work, audit trail, and inspection evidence.

Record ownership

Each page names which system owns the record, which team acts, and what Clinistack treats as operational evidence.

Permission-scoped views

Sponsors, CROs, Sites, and biotech teams can look at the same trial state without collapsing responsibility or exposing more than needed.

Inspectable records

Documents, signatures, access, denials, integration runs, AI suggestions, safety actions, and review decisions remain tied to audit evidence.

First rollout

Bring the study question your team keeps rebuilding.

We will review the product path, system context, owners, evidence, and rollout approach that fit the trial work in front of you.

Discuss your trial setup