FARMOVS Quality Assurance Division

Every detail matters

We realise how important the quality assurance (QA) function is in the clinical research process. Thus, our team of dedicated experts ensures that our clients receive the best service offering. The FARMOVS QA team is independent of our service units that conduct regulated activities. Its mission is to assess the compliance of clinical research activities proactively and independently, against current local and international standards of good practice (GxP) and other relevant laws and regulations.
As an independent group, QA identifies and highlights risks and risk trends through audit and inspection activities, and consultancy. They facilitate informed decisions to safeguard regulatory compliance and protect subject safety, data integrity and company reputation.

QA accomplishes this by utilising its experience and expertise to:
• Conduct audits and mock inspections
• Deliver expert compliance advice and consulting services
• Ensure the company is able to properly manage and host sponsor audits and regulatory inspections
• Report compliance issues to management and request actions to be taken to enhance operational excellence and process improvement to mitigate risk to the company and study sponsors

For more details email us:

Types of GCP Audits:

  • Protocol audit
  • Clinical Study Conduct Audit
  • Informed Consent Audit
  • Case Report Form Audit
  • In Process Audit
  • Database Audit
  • Clinical Study Report Audit
  • Investigator Site File / Trial Master File Audit
  • GCP Inspection Readiness Audit
  • Investigator Site Audit

Types of GLP Audits:

  • Method Validation and Bioanalytical Protocol audit
  • Method Validation and Bioanalytical Study Performance
  • Method Validation and Bioanalytical Reports

Contact Us

Charmaine van der Walt


Telephone:  051 410 3111

Carin Coetzee


Telephone:  051 410 3111