Precision
Quality
Integrity
Guided by science and purpose — we help life science organizations turn compliance into a meaningful part of their mission.
Beyond Compliance
At QM Advance, compliance is more than following the rules — it’s about understanding them and applying them in a way that makes sense for each organization.
We help companies build quality systems that are practical, consistent, and ready for inspection — without unnecessary complexity.
Good compliance supports good science. It protects patients, keeps products safe, and makes daily work easier and more transparent.
That’s why our focus is not just on meeting requirements, but on creating processes that people believe in and can rely on.
We work with teams across pharma, biotech, and tissue establishments to make compliance part of everyday quality, not a one-time effort.
Services
GMP & GDP Compliance
Tissue & Cell Establishments (SoHO)
QA of ATMP Manufacturing & Compliance
Quality Systems & Auditing
RP / QP Collaboration & QA Support
Regulatory Strategy & Compliance Advisory
Defined by quality
Committed to integrity
QM Advance provides quality and regulatory consultancy for the pharmaceutical, biotech, and tissue establishment sectors.
We help organizations build robust, inspection-ready systems that meet EU GMP, GDP, and SoHO requirements — with a focus on practical solutions and long-term sustainability.
Why choose QM Advance?
Because compliance should support your business — not slow it down.
At QM Advance, we focus on practical, effective quality systems that work in real operations and pass inspections with confidence.
We combine technical depth with hands-on industry experience to help you achieve and maintain compliance efficiently — without unnecessary complexity.
Whether you’re building a new QMS, applying for a GDP licence in the Netherlands, or need ongoing QA support, you get clear guidance, measurable progress, and peace of mind.
Each project represents a tailored, practical approach to achieving regulatory compliance and operational quality — across pharmaceuticals, medical devices, and tissue establishments.
We help organizations implement, optimise, and maintain systems that work in real operations and pass inspections with confidence.
Example outcomes:
- GDP licence successfully obtained within 6 months
- Tissue Establishment license obtained within 5 months
- ATMP QMS approved by Dutch Health Authorities (IGJ)
- ISO 13485 system restructured and re-certified with zero major findings
- QMS integration after merger of two European distributors