Our company manages both single-centre and multi-centre clinical studies in Bulgaria and participates in multinational clinical trials.
Clinic Design is fully equipped to meet the fast growing requirements of the industry for compressed timelines and operational and financial efficiency with promptness, precision, reliability and adherence to the high quality standards of the ICH GCP Guideline, Regulation (EU) 356/2014 of the European Parliament and of the Council and FDA Regulations Relating to Good Clinical Practice and Clinical Trials.
Our intelligent clinical methods aid the drug development process for our sponsors in the following areas:
• Monitoring of Clinical Trials (Phase I-IV)
• Regulatory Activities
• Medical Writing
• Site Management Activities
• Spectrum PV and Safety
• Training Activities Support
• Conduct of early phase trials in our own Hospital-based Clinical Research Unit for Phase I, BA/BE Studies
