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 email@example.com