Gaining Ethical Regulatory Authorities


To prepare and submit all required documentation to the national and international ethic and competent authorities.

  • Documents submission in Portugal (CEIC, CNPD, INFARMED) and in other European countries
  • Sites approval process
  • Oversee contract negotiations and development with participating sites
  • Follow-up of authorization process
  • Submission of amendments, progress and safety reports
© 2017 NOVA CRU. Todos os direitos reservados. Designed by NOVA IMS.