Study Start Up

We are committed to working with you to make the study conduct as straightforward as possible. We know, that a thorough preparation is a prerequisite for success and therefore emphasize planning and and scheduling. Pre study activities may include:

  • Planning of study design
  • Biometrical Planning
  • Feasibility
  • Development and design of the study protocol including informed consent
  • CRF Design / Database Design
  • Preparation of Investigator Site Files
  • Request for authorization to the competent authority
  • Request for opinion of the ethics committee
  • Notifications to local authorities
  • Public Registry
  • Preparation of all necessary study materials and organization of logistics, including shipment of study medication or sample transports

 

Algora delivers services and software for clinical research to industry and academic institutions.

  • Clinical trials phase II-IV
  • Non-interventional studies
  • Investigator initiated trials
  • Epidemiological research