Compliance That Keeps Pace With Your Ambitions
Regulators demand proof that every system behind a medicine is trustworthy. DQA makes that proof a competitive advantage — not a bottleneck.
Get in touch for a free consultation
30 years in pharmaceutical leadership | 15+ years experience per consultant | Deep expertise, not generalist advice | Clinical trial specialists | FDA and MHRA inspection-ready | GxP · GAMP 5 · 21 CFR Part 11 | GCP · GLP · GMP compliance | ISO 9001 certified | UK · EU · USA coverage | Trusted by clinical-stage biotechs and CROs | Oncology and rare disease expertise | CSV, CSA and data integrity experts | AI/ML compliance and system validation | Quality documentation and SOP development | Auditing and remediation | Quality and Regulatory Leadership | Short and Long Term Contracts |
What We Do
Many Areas of Expertise. One Standard of Delivery.
Wherever your challenge sits, the DQA Way applies: proportionate advice, hands-on experience, and a single expert who sees it through with you.
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Pharmacovigilance (PV) & GVP
Merger, Acquisitions & Due Diligence Support
AI/ML System Validation
Clinical Trial Systems Validation
Data Integrity
Quality Documentation & SOPs
GxP Auditing
Computer System Validation & CSA
Prepare for Inspections
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Have a specific challenge?
Global Coverage
Wherever You Operate, So Do We
Regulatory compliance doesn’t stop at a border, and neither do we. DQA supports clients across the UK, EU and USA from a senior-only team who work directly with sponsors, CROs and regulators across all three regions – no local hand-offs, no loss of context moving between jurisdictions.
In 2026 we extended that reach further, opening DQA China in Shanghai under local leadership. It’s the same standard, the same senior-led model, now closer to organisations running trials and manufacturing across Asia. Visit our China website.
Events
Where We Can Meet
Our team attend regular industry exhibitions. Here is where we will be:
ELRIG Drug Discovery 2026
We'll be there:
Wed
BioCap 2026
We'll be there:
Wed
- Thu
RQA 8th Global QA Conference
We'll be there:
Wed
Genesis 2026
We'll be there:
Thu
The DQA Way in Practice
What This Means for You
Mission, Motto, and Mantra aren’t wall art – they shape every engagement. That’s our way of working – our way of adding value to your organisation.
Every engagement follows the same disciplined, structured approach – the standard you’d expect from your own best people, applied consistently regardless of who on our team is leading the work.
You’ll deal directly with one senior consultant throughout, backed by a small team who already understand your business. No handoffs, no re-briefing a new face every quarter, no diluted advice passed down a chain. Just a direct, ongoing relationship with someone who thinks about your compliance position the way you do – as a peer, not a vendor.
That’s the DQA Way.
Our Mission
To make compliance an enabler of growth, not a barrier to it.
We deliver advice that is proportionate, practical, and grounded in real-world experience – so that regulatory compliance strengthens your business rather than slowing it down.
Our Motto
Built it. Audited it. Improved it.
Our team has operated from the inside of regulated environments – not just reviewed them. That means we know exactly where the risks are, and what genuinely effective solutions look like.
Our Mantra
One expert. One relationship. One standard.
You work with the same person from start to finish – no handoffs, no dilution of expertise, no surprises. The same high standard applies whether you’re a startup or a global pharma.
Who we work with
Our People
Experienced Specialists, Not Generalists
Our team is a small, deliberately curated group of practitioners - each with 15–25 years in regulated industries before moving into consultancy. No juniors, no volume. Across the team we cover every pillar of the DQA Way.
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Our Founder
The experience behind the DQA Way
Matt Jones
FOUNDER & PRINCIPAL CONSULTANT
After 30 years in pharmaceutical leadership — spanning auditing, quality strategy, technology implementation, and senior roles at globally recognised organisations — Matt founded DQA to deliver compliance that is pragmatic, proportionate, and genuinely fit for purpose. The DQA Way reflects how Matt has always worked: deep expertise, direct accountability, and advice calibrated to business reality as much as regulatory obligation. A long-standing TransCelerate contributor and published author on data preservation and provenance, he brings credibility earned from decades at the intersection of regulation and innovation.
Have a defined scope - or a challenge with no obvious solution?
Whether you need a targeted audit, a CSV programme from scratch, or a conversation about where Al fits in your validated environment, the DQA Way starts here.