Pharma & medtech / Compliant Scientific Promotion

Compliant Scientific Promotion

Promote products to professionals within applicable codes.

The problem

What is going wrong today

Promotional material is created without a clear review process, risking non-compliant claims under UCPMP and other codes.

Signs you need this

  • Material is used without medical review
  • Claims lack references
  • No record of approvals
What we do

The work, step by step.
Visible to your team.

Step 01

Set up a medical/regulatory review workflow

Step 02

Create templates with references and disclaimers

Step 03

Build a claim and evidence register

Step 04

Train marketing and field teams

The value

Better for your business.
Better for your customers.

The point of every solution is a better experience for the people you serve—and a business that runs more smoothly because of it.

Benefit to your business
  • Lower compliance risk
  • Faster approvals with clear steps
  • An auditable record of all material
Benefit to your customers
  • Doctors receive accurate, referenced information
  • Better-informed prescribing decisions
  • Patients protected from misleading claims
How progress is measured

Agreed measures.
Honest reporting.

Targets are set after the baseline—never a promised percentage on an unknown starting point.

Measure / 01

Material approval turnaround

Measure / 02

Claims with references

Measure / 03

Compliance findings

Product, medical, regulatory and legal review is required before publication. This is not a direct-to-consumer prescription-promotion package. No unsupported efficacy or safety claims.
Send an enquiry

Enquire about
compliant scientific promotion.

Tell us your situation. We confirm whether this solution fits and reply with a scoped first step.

Business information only. Please do not include patient, financial-account or other sensitive personal details.

Questions about this solution

Before you
enquire.

Still unsure? Ask us directly.

What does compliant scientific promotion solve?

Promotional material is created without a clear review process, risking non-compliant claims under UCPMP and other codes.

How does my business benefit?

Lower compliance risk Faster approvals with clear steps An auditable record of all material

What do my customers gain?

Doctors receive accurate, referenced information Better-informed prescribing decisions Patients protected from misleading claims

How long does it take?

4–6 weeks. Timing depends on scope, access and how quickly approvals come back.

Do you guarantee results?

No. We agree a baseline and measures first, deliver defined work and report honestly on what changed. Outcomes also depend on your team, pricing and service.