There are plenty of expert consultants with impressive CVs. So why me? Because I stay until the problem is actually fixed. Not until the report is written. Not until the invoice is sent.
Regulations are written in black and white. Real life happens in grey. That grey space — where science, risk, regulation and commercial reality intersect — is where I operate.
Experienced enough to understand regulatory risk. Modern enough to challenge outdated thinking.
Holding dual Master's degrees in Microbiology and Pharmaceutical Sciences from Kingston University London, with 18+ years of global experience, I have conducted 100+ GxP audits across 25 countries and built complete Quality Management Systems from the ground up.
Years Experience
GxP Audits
Countries
Built from Zero
I have supported organisations in progressing from zero infrastructure to holding their own MIA, WDA(H), and Specials licences. That journey is very different from maintaining an already mature system. It requires architecture thinking, regulatory strategy, and the ability to anticipate inspection challenges before they happen.
Companies don't need a walking GMP textbook. They need clear, decisive guidance on what to do now.
It's not about citing regulations — it's about interpreting them intelligently and applying them in a way that is practical and defensible under inspection.
I don't believe in isolated fixes. I look at the full end-to-end process, identify structural gaps, and strengthen the system as a whole.
Regulatory or compliance advice delivered without understanding commercial reality is incomplete — and ultimately immature.
I serve as QP, RP, and RPi across multiple organisations — not as a passive name on a licence, but as someone who personally reviews data, challenges investigations, certifies batches, signs declarations, and carries the responsibility that follows.
Dual Master's degrees in Microbiology and Pharmaceutical Sciences (Kingston University London). 18+ years of hands-on UK and global pharmaceutical experience spanning manufacturing, importation, wholesale distribution, and laboratory operations.
Independent QP, RP, RPi consultancy. GMP/GDP auditing. QMS architecture. Regulatory strategy.
Analytical testing, HPLC, method validation, batch release, quality systems management.
Supported companies from zero infrastructure to holding MIA, WDA(H), and Specials licences.
Whether you need a QP who actually reviews data, an RP who carries real responsibility, or someone to build your quality system from scratch — let's talk.
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