Our global team of highly experienced auditors provide GCP, GVP, GMP, GDP, GCLP, GLP and CSV auditing capabilities
Our processes include a technical peer review & QC check of all deliverable documents
to ensure quality and consistency
We provide a complete range of QA services with particular strengths in Pharmacovigilance (PV) and Good Clinical Practice (GCP).
We recognise that each of our clients has individual needs. With our tailor-made services, we have a broad range of expertise to meet your requirements. So much so, it would be difficult to list everything we do.
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Our global team of highly experienced auditors provide GCP, GVP, GMP, GDP, GCLP, GLP and CSV auditing capabilities, including the following:
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Global auditing
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Development and management of audit programmes
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CAPA management
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Risk management consulting on audit programmes
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Inspection readiness and post-inspection support
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Gap analysis
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Establishing PV systems for drug development and marketed products
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QMS development and review
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SOP writing and review
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Design, developing and delivering training
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In-house QA support