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Home · Solutions · Pharmaceutical companies
INDUSTRY SOLUTION · PHARMACEUTICAL COMPANIES

Between brand strategy and a prescription
sit seven minutes nobody sees.

Field force is the most expensive line in promotion and the least measurable one. NUMU CX makes the medical visit itself measurable: every conversation scored against your own model, cycle messages tracked to the doctor, compliance and adverse events caught the same day.

What is at stake

The company knows the visit happened.
Not what happened in it.

Double visits cover roughly one visit in twenty, and the rep behaves differently when the manager is in the room. Everything else reaches headquarters as a CRM entry written from memory in the evening.

~5%
of visits are ever observed

And those few are observed under conditions that change the behaviour being observed.

15–50%
gap between top and baseline reps

The same territory, the same portfolio, the same cycle materials — and a difference that nobody can currently explain with data.

24 h
the pharmacovigilance clock

A doctor mentions a suspected adverse event in passing. If the rep does not recognise it, the SLA is already running and nobody knows.

Who it covers

One quality standard
across every field role.

Medical representatives

Visits to doctors by specialty and category, with the visit model scored stage by stage and cycle messages tracked per brand.

Pharmacy representatives

Conversations at the counter, recommendation share, stock and display objections — the same scoring logic applied to the pharmacy floor.

Key account managers

Negotiations with chains, hospitals and procurement, with commitments and next steps captured rather than remembered.

Remote and call-centre contact

Remote visits and outbound calls scored against the same standard, so channels can finally be compared to each other.

What the platform reads

Pharma-specific, not a
generic script checker.

Your visit model

Pre-call through post-call, scored on the scale your trainers use, with the checklist calibrated against visits your own team has already run.

Brand and INN dictionaries

Your portfolio, competitor brands, dosages and therapeutic areas — so detailing time per brand is measured, not estimated.

Cycle key messages

Share of message per brand and per specialty, so the brand team learns mid-cycle which arguments are actually reaching doctors.

Adverse events

A suspected case is checked against the four validity criteria and routed to pharmacovigilance inside the 24-hour SLA, with the transcript attached.

Promotional compliance

Off-label claims, unsupported head-to-head comparisons, incentives and events offered in exchange for prescriptions — flagged in the same pass.

Coverage and frequency

Whether A, B and C category doctors are actually being seen at the planned frequency — verified against real visits rather than planned routes.

Data and regulation

Patient data never
reaches the database.

Masking happens before storage, not after. Capture of the other party stops without consent. The whole platform can run inside your own perimeter, which is what turns local data-residency and privacy requirements from a legal risk into a checkbox.

Role-based access means a rep sees their own visits, a first-line manager sees their team, and every access is written to an audit log.

PII masking
Names and patient details removed before anything is written
On-premise
Inside your perimeter, or an in-country cloud
AES-256
Encryption at rest, TLS in transit, retention you set
Local LLM
Available on request when nothing may leave the boundary
Where it shows up

Quality is the last lever
that still moves the number.

×1.5–2
visit-to-prescription conversion
+20–30%
sales at the same headcount
10 → 15–20
reps per first-line manager
100%
of visits under one review standard
Benchmark ranges for field-force quality programmes, not a guaranteed outcome. The 30-day pilot measures the range on your own visits and portfolio.
FAQ

Questions pharma field-force leaders ask first.

How is consent handled in the consulting room?

Capture of the other party stops if consent is not given, and that state is logged. Patient names and details are masked before storage — the architecture assumes the strictest reading of health-data rules from day one.

Can it really score against our own visit model, not a generic script?

Yes — your stages, your scale, your FABS structure and your cycle key messages, calibrated with your trainers during the pilot until the AI's scores agree with theirs on the same visits.

What happens when an adverse event is mentioned mid-visit?

The fragment is checked against the four validity criteria and routed to pharmacovigilance the same day, inside the 24-hour SLA, with the transcript attached — whether or not the rep recognised it in the moment.

How do reps take it — control or support?

Launches run coaching-only: scores visible to the rep and their first-line manager, not to HR. Reps get feedback minutes after the visit plus reference examples from teammates — which is why field teams end up defending the tool, not fighting it.

PHARMACEUTICAL COMPANIES

Start with one team.
Thirty days.

Eight to ten reps, your portfolio in the dictionaries, your checklist calibrated with your own trainers. It ends with a report on real visit quality, share of message and the compliance picture — plus a scale-up plan.