ethica CRO


Clinical
Study Management
Study Monitoring

Our full-service clinical monitoring is conducted in accordance with a well-designed monitoring plan, ICH-GCP Guidelines, applicable regulatory requirements, and our accredited SOPs.

Our on-site study monitoring services include:

  • Qualification visits (see Study Start-up)
  • Initiation visits
  • Study monitoring visits
  • Close-out visits

ethica Request a proposal

ethica Investigator Manual