Monitoring & Project Management

Our services:

  • Feasibility surveys
  • Selection and recruitment of study centers
  • Clinical Study Applications, CTA
  • Submissions to Ethic Committees
  • Selection and coordination of the central laboratory
  • Selection and coordination of further services
  • Creation and maintenance of the Study Master File
  • Creation of Investigators' Files
  • Initiation of study centers
  • Training of investigators and study nurses
  • Organization of Investigator Meetings
  • Patient recruitment support
  • Monitoring / Site Management
  • Management of study medication and material
  • Query Management
  • AE/SAE documentation
  • Closing of the study centers
  • Project management
  • Project administration
  • Insourcing / on-site support from our staff

 

Benefit from our know-how and well-established team synergies!

 

< Our Team

• 2022 – AMS are CTR- and MDR ready • 2022 – New unique AMS-ePRO® features launched • 2022 – Real-World Evidence focus in AMS Late-Stage Research • 2022 – AMS expanded its global reach • 2021 – DIGA dossier submission pioneer •

News