Your safety isn't a policy.
It's how we're built.

picking-the-perfect-dose-day

Every prescription we issue is governed by independently audited clinical standards, verified patient eligibility checks, and the same statutory regulators that oversee NHS providers (CQC, GPhC, MHRA, GMC).

Prescribing safety protocols

Clinical rigour behind every consultation

Our prescribing process is governed end-to-end by a clinical risk framework that's designed, audited, and continuously improved by our in-house clinical governance team. Our clinical governance processes are subject to independent external audit. Audit outcomes are reviewed by the Clinical Safety Officer and result in formal action plans tracked to completion.

Identity & Eligibility Verification

We answer to regulators, not just reviews

For weight loss medications, 2026 GPhC guidance requires prescribers to independently verify key patient metrics. Our verification processes were reviewed and updated to comply with the General Pharmaceutical Council's 2026 guidance on independent prescribing via digital services.

Here's exactly how we do that.

Every side effect report makes the system safer

You can report suspected side effects directly to the MHRA, or through us. Either way, it counts, and we actively use that feedback to improve

generalhealth

Report a side effect via Yellow Card

The MHRA's Yellow Card scheme is the UK's system for reporting suspected side effects, adverse drug reactions, and problems with medical devices, including faulty injection pens. You can report directly online, by phone, or through the Yellow Card app.

aboutushero

What to report

You can report suspected issues with:

Side effects or adverse reactions to your medication

Faulty or defective medical devices (e.g., a Mounjaro or Wegovy injection pen that jams or fails)

Unexpected changes in how a medication is working for you

Any other safety concern about a medicine or medical product

INTERNAL INCIDENT LEARNING

A learning culture

At Numan, patient-reported incidents aren't filed away; they're the most important input we have. Every adverse event triggers a structured clinical review that feeds directly back into our SOPs and prescribing processes.

Incident reviewed

Every reported incident is reviewed by the clinical governance team within a defined timeframe.

Root cause identified

We use structured root cause analysis to understand not just what happened, but why.

Protocols updated

Learning is translated into SOP updates, prescriber guidance, or patient communication improvements.

Regulatory & Professional Standards

Regulated, registered, and accountable

Numan operates under the oversight of the UK's healthcare regulatory bodies. Our compliance status is verifiable, because we think you should be able to check.

Service transparency

In line with GPhC requirements for online prescribing services, we publish the following information about our prescribing service.

Service addressFloor 4, Farringdon Point, 33 Farringdon Road, London, England, EC1M 3JF.
Prescriber typeDoctors (GMC-registered) and non-medical prescribers (GPhC AND NMC registered)
CQC registration1-6118870417
GPhC registration9011408

Clinical team

The people responsible for your care

GPhC guidance requires us to name the clinicians providing our prescribing service. All registration numbers are publicly verifiable on the relevant professional register.

Got questions about your care?

Our clinical team is here to help. If you have a concern about your treatment, a side effect, or anything about how we operate, reach out directly.

Updated: