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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.

Our global team of highly experienced auditors provide GCP, GVP, GMP, GDP, GCLP, GLP and CSV auditing capabilities, including the following:

  • Global auditing

  • Development and management of audit programmes

  • CAPA management

  • Risk management consulting on audit programmes

  • Inspection readiness and post-inspection support

  • Gap analysis

  • Establishing PV systems for drug development and marketed products

  • QMS development and review

  • SOP writing and review

  • Design, developing and delivering training

  • In-house QA support

Need more details? Contact us

We are here to assist. Contact us by phone, email or via our social media channels.

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