ethica CRO


Clinical
Study Management
Regulatory Affairs

Our regulatory affairs staff provides expert consulting and assistance to ensure that you are in compliance with the requirements of regulatory agencies worldwide, including:

  • Clinical Trial Submissions (CTA, IND)
  • Labeling of clinical trial materials
  • Regulations and guidelines governing clinical trials
  • Compliance audit services
  • Maintenance and archiving of documents

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ethica Investigator Manual