Monitoring at bioskin


bioskin's monitors/CRAs strive to maintain an excellent relationship with the investigator and site staff as well as the sponsor, ensuring that your trial runs smoothly and stays on schedule.  At the same time they guarantee that trials are conducted in accordance with the protocol, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) as well as applicable guidelines. 

Our monitoring services include:

  • Pre-study qualification visits
  • Site initiation
  • Organization of investigator meetings/trainings
  • Preparation and collection of regulatory documents
  • Clinical study logistic handling
  • Periodic site monitoring
  • Query resolution
  • Site termination
  • Risk based monitoring
  • Remote monitoring
  • Central monitoring

All services can be offered according to bioskin or sponsor SOPs.