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Recent Work
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CRC has been involved in a wide range of activities, these include:
- The auditing of clinical trial sites for pharmaceutical and biotech companies
and government organisations. These trials have covered a wide range of therapeutic
areas including Oncology (melanoma, renal cell carcinoma), Gastro Enterology
(inflammatory bowel disease), Cardiology (hypertension, angina pectoris), Virology
(hepatitis) and Rheumatology (rheumatoid arthritis) in human clinical trials and the
vaccination of wildlife against Tuberculosis in veterinary trials
- The pre-inspection and preparation of clinical trial sites for regulatory audits
- The creation and review of standard operating procedures (SOPs)
- The review of project specific procedures and CRO contracts prior to the start of
a clinical trial
- The creation and running of training courses. These courses have included sessions
on: data quality, questionnaire design, monitoring activities, the errors to avoid in
clinical trial design, the set up and management of clinical trials, monitoring
activities and effective data management
- The above activities have been undertaken in many countries, including: Argentina,
Austria, Belgium, Brazil, Canada, Czech Republic, Finland, Germany, Holland, Hungary,
India, Israel, Italy, Norway, Poland, Portugal, Romania, Slovakia, Spain, Sweden, Turkey,
Ukraine, UK and USA
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