Enhancing performance of investigational sites

Your problem

  • More than 80% of all clinical trials experience significant delays costing pharmaceutical companies upwards of $35,000 a day per trial.
  • Only about 7% of ALL sites actually deliver what they said they would do (in terms of enrolment) in the feasibility assessment.
  • For every two new physicians engaging in research practice this year, 1.5 will give up within two years.

Our approach

  • site management by identifying/monitoring key process inputs;
  • site risk management by identifying/eliminating potential failure modes/causes through preventive actions;
  • site performance predictability by process standardisation;
  • prioritisation of process improvement efforts by identifying the critical inputs;
  • development of a continuous improvement environment by implementing a Lean Six Sigma program;
  • consistency with the regulatory environment.

We help you

  • enhance the site's real operational performance and the site's performance predictability; 
  • reduce unneccesary site activations;
  • create a long-term relationship with the sites;
  • perform study planning more effectively and efficiently;
  • maximise the ROI in the site;
  • obtain high qualitative data based on a very effective Quality Management System.

Ezelstraat 69 | B- 8000 Brugge | Belgium | Phone: +32.50.33.33.40 | Fax: +32.50.33.33.39 | BTW BE 0866 039 556 | RPR/RPM Brugge | e-mail: info@hict.com