Quality Management, Auditing services to CRO pharmaceutical industry

CQC provides Quality Management and global Auditing services to the pharmaceutical and biotech industry:

all main types of GCP/GLP audits

of SOP- and Quality Management Systems

as external/interim Quality Management Function

of Regulatory Authority Inspections

More than 25 years of experience in quality management and GCP/GLP auditing

Diploma in Bio-Engineering, certified European Quality Manager (DGQ)

Head of Quality Management functions in two phase I CROs (Clinical Research Organisations) in Hamburg, Germany

Global Clinical Auditor for Schering AG, Berlin, Germany

Head of Clinical QA in the U.S. for Schering / Berlex / Bayer AG, Montville, New Jersey

Independent quality consultant since 2010 serving more than 100 clients, - small CROs to large global pharmaceutical companies

Member of German Quality Management Association e.V. (GQMA) and Deutsche Gesellschaft für Pharmazeutische Medizin e.V. (DGPharMed)

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