QMS
Quality Systems
Quality that works in the real world.
MEIA Consulting builds, maintains and improves quality systems for pharmacies and Life Science companies – from self-inspection programmes, SOPs and deviation management to complete GxP systems (GDP, GMP, GCP, GVP), audits and inspection readiness.
A quality system has to do two things at once: satisfy regulatory requirements and work in daily operations. Many systems only manage the first. MEIA Consulting builds quality systems around how your organisation actually works – industry understanding before standard solutions – and takes responsibility for keeping them alive through training, follow-up and ongoing management.
What we do
Quality systems for pharmacies
Self-inspection programmes, SOPs, deviation management, CAPA and training – built to work in daily operations, not just in the binder. The system is sized to your business and kept alive over time.
GxP systems for Life Science
Building and developing quality management systems according to GDP, GMP, GCP and GVP. We translate regulatory requirements into processes the organisation can actually follow – with clear ownership and traceability.
Audits and inspection readiness
Internal audits, supplier audits and gap analyses, plus structured preparation ahead of regulatory inspections. You get a clear picture of where you stand, prioritised actions and support in executing them.
Ongoing QA management
Quality work does not end when the system is in place. We offer ongoing QA support where we maintain, monitor and improve your quality system – as an integrated part of your operations.
Frequently asked questions
What does a pharmacy self-inspection programme include?
A self-inspection programme describes how the pharmacy ensures compliance with applicable requirements: procedures (SOPs), responsibilities, deviation management, CAPA, temperature and storage controls, and training. We build programmes adapted to your operations and easy to follow.
Which GxP areas do you work with?
GDP (distribution), GMP (manufacturing), GCP (clinical trials) and GVP (pharmacovigilance). We build new systems, develop existing ones and provide support during audits and inspections.
Can you help us prepare for a regulatory inspection?
Yes. We run gap analyses against the regulatory requirements, prioritise actions, prepare documentation and train the organisation ahead of the inspection.
What does ongoing QA management mean in practice?
An agreed, recurring QA engagement: we keep documentation current, drive the deviation and CAPA process, follow up key metrics and run periodic reviews – so the quality system evolves with the business.
Relevant forPharmaciesLife ScienceDigital health