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NquiRx

From in bullet points to in-field in hours, not weeks.

NquiRx helps pharma insights teams go from a study brief to a launched survey with routing and logic, plus a collaboration workflow to collect stakeholder feedback directly in the work-in-progress survey—powered by today’s leading AI models.

Request a demo See what you get

Built for pharma insights teams; designed to fit real-world market research workflows.

Faster cycles, lower effort, and fewer handoffs.

If you run primary market research in pharma, you know the bottleneck is not “coming up with research ideas”; it is getting from a brief to a build that is ready to field, with logic that survives review and revisions.

Faster build cycles

Get from brief to a launched survey quickly; iterate without losing logic or structure.

Review without chaos

Share a link to the work-in-progress survey so stakeholders can leave feedback in one place; avoid scattered edits across decks and email threads.

Built for pharma workflows

Designed for real review cycles; keeps assumptions and logic explicit.

What you get

End-to-end survey management, plus a shared workflow for review and iteration.

End-to-end survey build and launch

Turn a brief into a survey that is ready to go in-field, with routing and logic implemented and managed in one place.

Stakeholder collaboration in the survey

Send a single link to the work-in-progress survey so reviewers can comment where it matters; keep feedback tied to specific questions and logic.

Real-time visibility and clean exports

Monitor response progress as data comes in and export respondent-level data to CSV for analysis in Excel or your own stack.

Designed for compliant pharma market research

  • Designed to support compliant US market research workflows and participant protections.
  • Aligned with industry standards for ethical research and data protection practices.2
  • Built to fit your SOPs and review process; routing and assumptions stay explicit.
Workflow traceability Stakeholder collaboration Audit-friendly outputs Designed for SOPs

Compliance is a shared responsibility; we collaborate with your legal, privacy, and insights teams to fit your requirements.

Product preview

Screenshots coming soon; placeholders below show the intended workflow.

Placeholder preview of an intake wizard capturing research objectives and constraints
Brief intake
Placeholder preview of a question list editor showing routing and logic annotations
Question, logic, and collaboration
Placeholder preview of logic and survey specification output for programming
Routing and launch preview
Placeholder GIF showing end-to-end survey workflow from brief to programmed output
End-to-end flow (GIF placeholder)

How it works

NquiRx follows a structured build workflow; it automates the parts that usually take the most time and creates a single workspace for review, iteration, and launch.

01

Start from your brief

Provide objectives, audience, and constraints; add optional background if helpful.

02

FDA data grounding1

NquiRx uses FDA public data to keep AI-driven survey design relevant and grounded.

03

Clarify and draft

NquiRx asks targeted follow-ups, then drafts a question set with routing and logic.

04

Collaborate and iterate in one place

Share a link to the work-in-progress survey so stakeholders can comment directly; routing stays explicit across revisions.

05

Launch and manage fielding

Launch the survey, monitor progress as responses arrive, and export a clean respondent-level dataset.

See it on your next study brief.

Request a demo
  1. Public data sources: ClinicalTrials.gov API; FDA Access Data.
  2. Insights Association Code of Standards and Ethics.