Why ClaripHy™ GxP

A team built from the industry we serve, not around it

Decades of pharmaceutical GxP experience, brought together to build something fairer, faster and more human.

85+
Years combined GxP experience
1,750+
Pharmaceutical clients worked with
1,000+
Audit reports under our leadership
25
Years of client-side quality leadership

ClaripHy™ GxP was founded by professionals who helped build the modern third-party pharmaceutical auditing market.

Our experience spans the client, commercial, operational and technical sides of the industry, giving us a perspective that very few organisations can offer.

Collectively, our founding and core team bring more than 85 years of direct pharmaceutical GxP experience, complemented by senior leadership in Regulatory Affairs, technology and other highly regulated industries.

Rather than viewing pharmaceutical auditing from a single perspective, our experience has been built across every stage of the audit lifecycle.

Client-side quality leadership

For 25 years, a member of our team served as Quality Director for a major French pharmaceutical Marketing Authorisation Holder, commissioning supplier audits, managing external audit providers, implementing audit findings and taking responsibility for the compliance decisions that followed.

That experience gives us a genuine understanding of what clients need from an audit because we have sat on the receiving end of them for a quarter of a century.

Commercial leadership across global markets

Our commercial leadership includes more than a decade in senior client-facing and key account roles at one of the pharmaceutical industry's most established GxP audit providers.

During that time, our team worked directly with more than 500 pharmaceutical companies, sold thousands of individual audits and personally built approximately one-third of that provider's audit library from the ground up.

They also transformed France into one of its strongest-performing markets.

Across our wider commercial team, we have worked with a further 1,250 pharmaceutical clients, driven significant commercial growth throughout the DACH region and generated multi-million dollar revenues across the United States market.

These are not theoretical market insights. They are the result of decades of delivering measurable commercial success across Europe and North America.

Operational excellence in audit delivery

Our team includes the production leadership behind a competitor's audit business as it scaled beyond 1,000 completed audit reports.

That experience includes personally overseeing the delivery of thousands of audit reports from initial completion through CAPA management to formal audit closure, ensuring quality, consistency and reliability throughout the entire process.

Our wider operational team contributes a further decade of hands-on audit delivery experience across thousands more reports, providing the operational depth required to deliver complex audit programmes at scale.

Regulatory Affairs expertise

Beyond auditing, our leadership also brings extensive Regulatory Affairs experience, including leading an international market expansion programme into Ireland for a major multinational pharmaceutical organisation.

This broader regulatory perspective strengthens our understanding of the commercial and compliance environments in which our clients operate.

Technology built to support experts

Our Chief Technology Officer brings extensive senior technical leadership experience to the development of ClaripHy™ GxP's technology platform.

Our systems are designed to make audits faster, more efficient and easier to manage without compromising the professional judgement that pharmaceutical quality demands.

While many organisations are moving towards AI-generated compliance outputs, we believe technology should support experienced professionals, not replace them. Pharmaceutical quality remains, first and foremost, a human responsibility.

Our purpose

Why we built ClaripHy™ GxP

After decades working within the established pharmaceutical auditing market, we believed clients deserved something better: greater transparency, fairer pricing, faster delivery and a partner focused on long-term relationships rather than volume alone.

ClaripHy™ GxP was created to deliver exactly that.

Working with us

What this means for you

More than 85 years of direct pharmaceutical GxP experience.
25 years leading quality within a pharmaceutical Marketing Authorisation Holder.
Direct commercial relationships with more than 500 pharmaceutical companies, with thousands of audits sold and delivered.
A further 1,250 client relationships across France, the DACH region, the United States and wider international markets.
Production leadership through the delivery of more than 1,000 completed audit reports, including full CAPA management and audit closure.
Thousands of additional audit reports delivered across our wider operational team.
International Regulatory Affairs leadership supporting multinational pharmaceutical expansion.
Senior technology leadership developing a modern, efficient audit platform built specifically for pharmaceutical quality.

We have taken decades of experience and built something different: a consultancy that is more responsive, more transparent and more human.

Because every audit ultimately supports the people who matter most: the patients who rely on medicines manufactured to the highest standards of cGMP.

Work with ClaripHy™ GxP

Experienced people. Clear advice. Better audit outcomes.

Speak directly with our team about your audit, quality or compliance requirements.