Hallam Pharma Consulting specialises in conducting GCP audits of clinical trials in phases I to IV and vendor qualification audits.  Since 2000 we have conducted audits in Europe and beyond, including the following countries: UK, Eire, France, Germany, Denmark, Finland, Sweden, Norway, Poland, Czech Republic, Hungary, Switzerland, Spain, Portugal, Netherlands, Greece, Belgium, Austria, Ukraine and USA.

We conduct audits of:

  • Trial Master Files
  • investigational sites
  • clinical study reports
  • archive facilities
  • phase I units
  • database and data management.

Audits have been undertaken on behalf of pharmaceutical companies, CROs, academic sponsors, NHS Trusts and charitable organisations.

Further information available from info@gcp-quality.com