Solutions
You came here for help with a specific grind, whether that's the study-build crunch, the query backlog, or the week before an inspection. Tell us where you sit and we'll point you to the exact agents that lift it, with you in control the whole way.
Not sure which fits?
You do not have to know whether you are an “organization” or a “role” to get help. Find the grind below that sounds most like your week, then jump into the path it points to. The relevant agents are already mapped there.
The protocol is locked and first-patient-in is on the calendar, but the database, CRFs, and edit checks still aren't built. Every day of setup is a day borrowed from enrollment.
Often a Data Manager or Database Designer starting point
You close ten queries and twelve more open. Cleaning drags into the evening, and database lock keeps sliding to the right while the same discrepancies come back around.
Usually a Data Management role starting point
Six weeks to the inspection and the eTMF still isn't complete. Documents are missing, misfiled, or unsigned, and no one can say with confidence that the file is ready.
Often a QA, Regulatory, or Sponsor / CRO starting point
The SAP is signed, the mock shells are approved, and now someone has to program, QC, and reconcile table after table after table, under a timeline that assumed none of it would slip.
Usually a Biostatistics or Statistical Programming starting point
A serious event lands and the clock starts. Case intake, MedDRA coding, expedited reporting, and reconciliation against the clinical database all have to be exact, and the regulatory deadline does not move.
Often a Pharmacovigilance / Safety role starting point
Work is scattered across a CRO, point tools, and spreadsheets, and every handoff is a place where things get dropped, duplicated, or lost. You own the outcome but not the pieces.
Usually a Sponsor, CRO, or Biotech starting point
A qualified person reviews and approves every one of these. The agents draft and detect; you stay in control.
Start where you sit
Same platform, seen through your day. Pick the lens that fits and we've already done the mapping, from the pain you feel to the outcome you're after to the agent that gets you there. No hunting required.
By organization
Sponsors, CROs, research sites, and emerging biotechs each carry a different mix of in-house capability and outside vendors. The organization view re-packages the 37 agents around the outcomes you are accountable for, from first study start-up to a submission-ready dataset and an inspection-ready eTMF.
4 tailored solutions below
By role
Data managers, biostatisticians, medical writers, monitors, regulatory and QA, project managers, and safety teams each feel a specific bottleneck. The role view foregrounds the agents that take the repetitive weight off your day so your time goes to judgment, not keystrokes.
7 tailored solutions below
Still not sure which lens? If you are scoping the platform for a whole company, start by organization. If you own one function and want the bottleneck in your day gone, start by role. Most teams read both, and it is the same platform either way.
See where NeogeniQS fits your organization and your role.
By organization
By role
One platform underneath
Solutions are a lens, not a separate product. Behind each persona page are the same four suites (Study Build & Design, Data Management & Oversight, Biostatistics & Reporting, and Documents, Ops & Support) running with human-in-the-loop review and full traceability.
Built for regulated trials, whoever you are
Whichever path you choose, the same guardrails hold. Every agent runs with a person in the loop, grounds its output in your source documents, and leaves a full audit trail. No black boxes, no lock-in, and while we're pre-launch, we're honest about the limits.
No pitch and no pressure. You get a working walkthrough on your own workflow and straight answers, limits included. Bring your hardest study.
