Rightview puts cited, protocol-grounded answers in front of the people who run your trial, and automates the work around them: custom reports, site budgets, amendments and source review. Every action is approved by your team.
| Site | Enrolled / plan to date | IRT check | Status |
|---|---|---|---|
| Site 001 | 14 / 14 | Matches | ✓ On track |
| Site 007 | 9 / 12 | 1 mismatch | ! Behind 25% |
| Site 012 | 12 / 13 | Matches | ✓ On track |
| Site 019 | 5 / 8 | Matches | ! Behind 38% |
Coordinators hit protocol problems first. Rightview sees them as they happen, handles the operational work around them, and shows you what every site is running into.
Protocol, amendments, IB, lab and pharmacy manuals, ICF, budgets and CTAs. One sponsor-controlled collection, kept current at every site.
Every answer and every check cites the exact page in your study documents, so anyone can verify it in one click.
Reports, budget reviews, pre-screening, SAE handling, source review and amendments run in seconds instead of days.
Nothing reaches a site, a subject record or a sponsor system until a person on your team signs off.
HIPAA BAAs, PHI auto-redaction, independent audit in progress. 21 CFR Part 11 tamper-evident audit trail, e-signatures and least-privilege access.
Rightview is the first line for operational study questions from investigators, site staff, CROs and your own team, with insight from a single study up to your program.
Site staff get answers and checks grounded in your study documents, so every site gives the same answer and works from the same source of truth.
Pre-screening against the real inclusion and exclusion criteria, with the citation, so ineligible patients are caught before they cost a screening visit.
Source is checked against the protocol before it reaches the eCRF, with every write approved and logged. Fewer queries for monitors and data managers to chase.
Adverse events are captured, classified against the protocol and escalated to the PI in minutes, not days.
Fewer deviations, missed visit windows and open queries at the end means less cleanup between last patient out and lock.
Checked in under 30 seconds, with the citation for every criterion.
Ask for the report you need in plain language. Rightview builds it from live study data, cross-checks IRT and other sources, and exports it ready to share with your study team and partners.
Describe the report you need. No template requests, no waiting on a data team.
Site activity checked against IRT and other sources in a single answer.
Live status for enrollment, visits and open issues, with forecasts.
From one site to your full portfolio, with studies compared side by side.
| Site | Enrolled / plan to date | IRT check | Status |
|---|---|---|---|
| Site 001 | 14 / 14 | Matches | ✓ On track |
| Site 007 | 9 / 12 | 1 mismatch | ! Behind 25% |
| Site 012 | 12 / 13 | Matches | ✓ On track |
| Site 019 | 5 / 8 | Matches | ! Behind 38% |
Rightview validates each site budget against the protocol, drafts counter-proposals within your guardrails, and sends every position to your team for approval before it goes out.
One amendment can touch every site, every enrolled subject and every budget line. See what it hits before it spreads, with no re-keying schedules site by site. The same flow keeps every site on the current ICF, lab manual and other study documents.
To every site enrolled in the study.
A per-site summary of the sites, visits, subjects and eligibility rules the change touches.
Schedule of assessments, visit schedule and eligibility checks update from the effective date.
Per-subject changes are reviewed before any write. Every change is logged and every acknowledgement tracked.
Nothing changes in a subject record until your team approves it.
Rightview collects what sites run into across your study, so you can benchmark your design against comparable protocols and fix ambiguity and burden before they become deviations, dropouts or an amendment. Then take the same signal into your next design.
See which criteria cost you the most patients, site by site.
Find windows that are too tight to run in practice.
Spot steps that are skipped, delayed or interpreted differently.
Repeated questions point to unclear text. Clarify it before it becomes a deviation.
Most asked questionDoes the 8-week washout start from the last dose or the last infusion visit?
Set the hours your team and your sites spend on each workflow every month. We apply the estimated speedup for each one, using the low end of any range.
Applies the estimated speedups to the hours you enter. An estimate, not a guarantee.
Your science, our technology. Here is how a pilot runs.
Choose the study, sites and workflows, and load your study documents.
Bring your study team and sites onto Rightview.
Review the results against the goals set during scoping.
Continued support, with value tracked through the study.
Upload your study documents and every site has access immediately. No IT integration, no site-by-site training.
Request a Pilot