Responsible Person (import) — RPi Services UK

Verification-system governance for eligible medicinal products imported into Great Britain

Scope of RPi Support

Ensuring qualified person certification and batch-release compliance for imports.

Scope Review
A professional reviewing pharmaceutical import documents with a laptop and notes.
A professional reviewing pharmaceutical import documents with a laptop and notes.

Assess import routes and licence scope against MHRA guidance.

Close-up of hands verifying certification paperwork for medicinal products.
Close-up of hands verifying certification paperwork for medicinal products.
A team meeting discussing batch-release and quality control procedures.
A team meeting discussing batch-release and quality control procedures.
Verification Checks

Confirm QP certification and batch-release evidence where applicable.

Manage deviations, CAPA, change control, and maintain inspection readiness.

Ongoing Oversight

FAQs

When is an RPi required?

An RPI is needed for importing eligible medicines into Great Britain.

What evidence is checked?

Verification includes QP certification, batch-release data, and supplier due diligence.

Can checks be delegated?

Delegation is possible but the RPI retains oversight and accountability for all checks.

How is the system audited?

Through self-inspection, management review, and periodic reporting processes.

Who can be formally appointed?

Appointment depends on eligibility, MHRA acceptance, and licence holder’s process.

How does engagement with WinnPharma work?

We review scope, design or assess gaps, remediate, implement, and provide ongoing oversight.

Get in Touch

Questions about RPI services? Reach out anytime for clear, practical answers.

P

+44 1234 567890

E

contact@winnpharma.co.uk