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, Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 and FDA Regulations Relating to Good Clinical Practice and Clinical Trials.

  • Monitoring of Clinical Trials (Phase I-IV)
  • Regulatory Activities
  • Medical Writing
  • Site Management Activities
  • Spectrum PV and Safety
  • Training Activities Support
  • Conduct Early phase Trials in our own Hospital-based Clinical
  • Research Unit for Phase I, BA/BE Studies

About us

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Our Mission

Our mission is to be an agile and attentive partner offering unique access to full service, global support but with outstanding customer service...

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Our Strengths

Among Clinic Design’s strengths are its flexibility and innovative approach which contribute largely to clinical research and make the company a pref..

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Our Team

Our team provides all clients with professional, competitive and completely confidential service of the highest quality. In pursuance of that aim and..