Vendor Auditing
Vendor Quality Audits for GxP environments
In addition to our IT specialism with audit experience since 2004, we perform vendor quality audits for GCP, GMP, GLP and GPvP, we can deliver, qualification, routine or for cause vendor audits on your suppliers from CROs, to laboratories and IT supplier, we can help you assess your vendors capabilities, quality management, compliance and suitability.
- Supplier Qualification.
- Analytical & Clinical Laboratories.
- Contract Research Organisations.
- IT Suppliers and Data Centres.
Our auditing services include:
- Development of Audit Plans / Agendas.
- Conducting Onsite Audits (either as Lead Auditor or team member).
- Audit Observation Write-up and Reporting.
- Review of Auditee CAPA Responses.
We are a UK based Pharmaceutical Consultancy specialising in Data Integrity, Computerised System Validation and IT Quality Assurance services. TS CSV QA’s mission is to deliver pragmatic fit for purpose solutions to our clients to support technological implementation and innovation in the Pharmaceutical and Healthcare sectors. Founded by Trev Simmons, Trev is a Fellow of the Research Quality Association, and an active member of the association, and is currently Chair of the Digital Information Governance and Information Technology (DIGIT) Committee as well as the Cross-GxP Working Party on Data Integrity.