About CQMP

Built by compliance professionals, for compliance professionals.

CQMP was founded on a simple belief: regulated industries deserve compliance partners who understand the science, the regulations, and the real-world pressures of getting products to market safely.

30+
Years of combined experience
200+
Validations completed
100%
Audit pass rate
50+
Clients served

Our story

From the lab to the boardroom — we've been there.

CQMP was founded by industry veterans who spent years inside pharmaceutical and biotech organizations — writing protocols, managing audits, and navigating the complexity of FDA and EU GMP requirements firsthand.

We built CQMP because we saw a gap: companies needed compliance partners who could think strategically, not just execute checklists. Partners who understood that a missed validation step isn't just a documentation problem — it's a patient safety issue, a business risk, and a regulatory liability.

Today, CQMP serves clients across the pharmaceutical, biotechnology, medical device, and clinical research sectors — delivering validation, compliance, and project management services that hold up under the toughest scrutiny.

Our commitment
Every engagement, every time
  • Inspection-ready documentation
  • Risk-based, practical approach
  • Regulatory expertise on call
  • Long-term compliance partnership
  • Compliance-aware project management
100%
Audit pass rate

What drives us

Our values

Integrity first

We never cut corners. Every deliverable we produce is one we'd be comfortable defending in front of an FDA inspector.

Partnership over transactions

We invest in understanding your organization so our work fits your culture, your systems, and your goals.

Practical expertise

Regulatory knowledge is only valuable when it's applied intelligently. We translate complex requirements into clear, actionable plans.

Continuous improvement

The regulatory landscape evolves. We stay current so our clients always have guidance grounded in the latest guidance and best practices.

Credentials & expertise

Regulatory expertise you can rely on.

Our team maintains deep, current expertise across the regulatory frameworks that govern your industry.

FDA 21 CFR Part 11
Electronic records and electronic signatures compliance
EU GMP Annex 11
Computerised systems in regulated environments
GAMP 5
Risk-based approach to compliant GxP computerised systems
ISO 13485
Quality management systems for medical devices
ICH Q10
Pharmaceutical quality system guidance
ICH Q9
Quality risk management principles

Ready to work with a team that gets it?

Let's talk about your compliance challenges and how CQMP can help.