Cromos Services

Clinical Trials:
  Project management
  Feasibility studies
  Submission to ethics committees
  Submissions to regulatory authorities
  Verification and collection of regulatory documents
  Organization of investigator meetings
  Monitoring of clinical trials
  Safety reporting
  Shipping, distribution and storage of trial supplies including customs clearance
  Adaptation of study documents in accordance with national legislation
  Translation of study documents into local language
  ICH GCP training for CRAs and investigators
  Site personnel training

Pharmaceutical Consulting Services:
  Custom Consultancy
  Regulatory Consultancy Services

Regulatory Services

Training

Monitoring

Trial Supplies

Quality Assurance