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Healthcare professional reviewing a checklist, verifying quality and compliance requirements in a clinical setting

Synergy Biologics
MIA(H) Services

UK Importation & Qualified Person (QP) Batch Release.

​UK Importation & Qualified Person (QP) Batch Release.

Synergy Biologics provides MHRA-authorised MIA(H) Importation and Qualified Person (QP) batch release services for licensed medicinal products entering the UK. We act as a UK regulatory gateway for international manufacturers and Marketing Authorisation Holders, enabling compliant UK supply without the need for clients to hold their own MIA licence or employ an in-house QP.

Healthcare professional reviewing documentation to approve batch release, checking GMP requirements & quality control records

Our Regulatory Scope

Operating under an MHRA Manufacturing & Import Authorisation (Human) - MIA(H), we are authorised to:

  • Import licensed medicines into the UK.

  • Perform QP batch certification.

  • Release products for lawful UK supply.

  • Operate under full UK GMP oversight.

What Our MIA(H) Service includes

UK importation of licensed medicines.

QP batch review and certification.

GMP documentation verification.

Regulatory documentation management

MHRA inspection readiness.

Recall, deviation and incident support

MIA(H) Import & Release Pathway

  1. EU-GMP manufacture

  2. UK import under our MIA(H)

  3. QP batch certification

  4. Legal release for wholesale supply

  5. Optional GDP-compliant storage & distribution under WDA(H)

MIA(H) import of supplement boxes at Synergy Biologics, illustrating MHRA-authorised handling, inspection

Who This Service For?

International pharmaceutical manufacturers

EU manufacturers supplying the UK post-Brexit

Marketing Authorisation Holders without UK infrastructure

Niche and specialist medicine suppliers

Virtual pharmaceutical companies

Business handshake symbolising partnership agreement, professional collaboration and trusted B2B relationships

Commercial Benefits

  • No UK entity required

  • No in-house QP needed

  • Faster route to UK supply

  • Reduced regulatory burden

  • Immediate access to MHRA-authorised infastructure

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QP Oversight & Patient Safety

All batches are certified by a UK-registered Qualified Person, ensuring compliance with the Marketing Authorisation, UK GMP and MHRA requirements.

Integration with Other Licensed Services

Our MIA(H) services integrate seamlessly with:

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  • WDA(H) for GDP-compliant storage and distribution

  • UK regulatory and market-entry support

  • EU-GMP manufacturing partners

Discuss UK Import & Batch Release

Planning UK market entry for a licensed product? Our team can guide you through importation, QP release and compliant supply.

MIA(H) Services Form

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