Accord Research offers a fully comprehensive training tender and can prepare a full scale bespoke teaching and training program for our clients in any of the following areas:

  • GCP standards
  • Investigator’s responsibilities and study obligations 
  • Monitoring
  • Legal aspects of the clinical trial  
  • Administration of the clinical trial 
  • Protocol and study methodology and conduct

Our educational programs are an essential part of each clinical study and by law all study participants have to be adequately trained in ICH GCP and all study-related procedures. The training program, proposed by Accord Research, is primarily dedicated to the following study participants:

  • Investigators and investigational research staff
  • Other study site staff e.g. pharmacy
  • Monitors
  • Study administration support

The courses may be prepared and taught directly by Accord Research experts or together with Sponsor representatives.