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:

  • 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.

Europe: t. +44 1235 854033 | Singapore: t. +65 6408 3766 | USA: t. +1 617-401-2630

e. info@zigzagassociates.com | Zigzag Associates Ltd

 Registered Office: The White House, Mill Road, Goring on Thames, Reading, Berkshire, RG8 9DD, UK

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