AI workflow software for pharma quantitative primary market research

From study brief to PowerPoint report faster and easier.

NquiRx gives pharma insights teams one place to build, field, manage, and report quantitative research. Nquirer, its AI agent, works across the study to create drafts, prepare revisions and fieldwork follow-ups, and produce analysis outputs—while your team controls approvals and final decisions.

Book a demo See the workflow

One connected study recordNquirer AI agent across the studyAutomated fieldwork managementPowerPoint + Excel outputs

From brief to report

Intake form / RFP upload Study context and clarifications start the record

Draft review Screener and questionnaire edits stay attached

Program and launch Survey logic and hosted respondent links move together

Fieldwork and exports Vendor coordination, response exports, and open-end signals stay visible

See the full study journey.

From study need through PowerPoint and Excel outputs, NquiRx keeps context and decisions connected. Give Nquirer a goal and it uses that live study record to prepare work across stages, pausing at the human decisions and approvals you configure.

Illustrative study workflow

One example study, with Nquirer working across connected stages.

Nquirer AI agent for your study workflow Run Nquirer across the connected workflow, or use any action below yourself. It carries out eligible work within the permissions and approval gates you set.

Ready to run

Stage 1 Study setup Brief ready

Stage 1

Study setup

Brief ready

Objective

Evaluate blinded oncology HCP concept preference.

Audience

US and Germany HCPs, oncology focus.

Materials

Stimulus attached, draft screener notes captured.

Timing

Launch-ready draft needed this week.

Screener outline

Eligibility, specialty, market, and concept-exposure checks prepared for review.

Questionnaire draft

Profile preference, rationale, and open-end probes organized into a first draft.

Review notes

Assumptions and open clarifications surfaced before stakeholder review.

Creating review-ready draft...

Stage 2 Questionnaire review Ready

Stage 2

Questionnaire review

Ready

Oncology HCP concept test

Q12. Which product profile would you be most likely to consider for appropriate patients?

Reviewer comment

Clarify that the profile is blinded and keep the attribute order consistent across markets.

Prepared revision

Use blinded product profile wording, keep the attribute order consistent, and apply the update across the master draft and Germany market version.

Prepared

Preparing the revision...

Stage 3 Fieldwork management In field

Stage 3

Fieldwork management

In field

Panel partner A

Open questions

Feasibility questions need an owner-ready follow-up before recruitment can move cleanly.

Drafted follow-up

Can you confirm feasible incidence by market, target completes by Friday, and any exclusions needed for the blinded profile review?

Preparing the owner-ready vendor follow-up...

Stage 4 Analysis and reporting Ready for analysis

Stage 4

Analysis and reporting

Ready for analysis

124Completes

3Markets

18Open ends

Profile preference

Slide ready

Profile A

64%

Profile C

31%

Open-end signal

Needs analysis

Comments cluster around access, dosing simplicity, and confidence in the safety profile.

Generated open-end analysis

Theme

Access and affordability language appears in 9 of 18 comments.

Profile A

Dosing simplicity is the strongest positive driver.

Automated AE/PC flags Review needed

2 potential AE/PC mentions flagged for human review.

Human review required

Preparing analysis outputs...

What changes

Faster, expert-led market research.

NquiRx keeps the study record, approvals, programming, fieldwork, and outputs connected. AI takes care of routine work and handoffs while researchers retain methodological judgment, approvals, and final interpretation.

Without NquiRx

Briefs, comments, and vendor instructions move between separate files and threads.
Questionnaire programming and launch require repeated handoffs and re-briefing.
Fieldwork updates, exports, and reporting begin outside one shared study record.

With NquiRx

Structured study context carries forward into a fully programmed survey.
Review history, hosted links, and vendor updates stay attached to the study.
PowerPoint reports and Excel outputs begin from the connected study record.

Team fit

Built for the teams behind pharma quantitative primary market research.

Whether you own the study, deliver it, or make fieldwork happen, NquiRx gives each team clearer workflow context around the work they already lead.

Panel and fieldwork firms

Add a higher-value study workflow capability around the respondent access and fieldwork execution your clients already rely on.

Package panel recruitment with clearer questionnaire review, launch, and reporting context.
Give clients a smoother path from approved materials to fieldwork status.
Offer a stronger service layer without rebuilding your delivery model.

Pharma MR consultancies

Consulting teams can accelerate the current study process, reduce manual coordination, and protect expert review time.

Keep the brief, screener, questionnaire, and reviewer decisions connected.
Spend less time translating comments, vendor instructions, and field updates.
Preserve methodology ownership while lowering delivery cost and churn.

Pharma commercial and insights teams.

Bring the work around each quantitative study into a clearer review and delivery flow from study need through reporting.

Give stakeholders a clearer way to review and approve study materials.
Reduce the spreadsheet and email load around launch readiness.
Give analysts a cleaner starting point, with study context and outputs carried forward together.

Built for the standards of pharma market research.

Approval gates, configurable respondent-facing legal and compliance language, reporting routes, and a study history keep participant protections, review, and coordination clear across insights, legal, privacy, and fieldwork partners.

Approval gates before launch Automated AE/PC pharmacovigilance reporting Configurable respondent-facing legal and compliance language Auditable study history

Founder-led demo

See how NquiRx fits the next pharma MR study your team needs to deliver.

Book a demo ...or message us on LinkedIn