Successful management of your clinical trial (phase I – IV):

  • Initiation, monitoring and closeout visits of clinical trials
  • Recruitment and selection of investigator sites, feasibilities
  • Obtaining ethic approval and approval of regulatory authorities
  • Preparation and maintenance of investigator site files
  • Preparation and maintenance of trial master files
  • Design, composition and print production of information material (e.g. poster, hand-outs, advertisements, product information, package inserts)
  • Audit preparation
  • Training of study staff
  • eCRF training