GMP quality assurance
A quality system that lives on the shop floor and withstands an inspector’s scrutiny.
A robust quality system is more than procedures: teams must understand it and apply it every day.
POMEX helps pharmaceutical, biotech and medical device sites strengthen their GMP quality system with hands-on consultants. We work with production sites in Wallonia (Hainaut, Walloon Brabant, Namur, Liège), Brussels and northern France.
What we do
We work on the key quality assurance topics:
- internal and supplier audits, GMP and ISO compliance reviews;
- deviation management, investigations (root cause analysis) and CAPA follow-up;
- review and simplification of documentation: procedures, work instructions, forms;
- inspection readiness, support during the visit and responses to observations;
- training teams in good practices and quality culture.
Our added value
Our strength: turning an audit finding into a concrete action plan, with owners, deadlines and indicators, rather than a pile of extra documents.
How we work
Depending on your needs, our consultants work:
- alongside your quality teams;
- as an interim replacement for a key role;
- on a targeted remediation project.
The expected result
A simpler quality system, better applied and ready for the next inspection.