Regulatory Support

GAIC provides support to clinical studies submission to the CAML Ethics Committee  by: 

  • Managing documentation collection and revision required for EC submission (e.g. Study Authorization Letter, Investigator’s CV, EC questionnaire, etc.);
  • Reviewing and ensuring the follow-up of all the submission process until all required approvals are obtained;
  • Amendments and reporting management. 

Please check CNPD requirments.

Please contact us prior to Centre submission to obtain the updated checklist of documents and necessary templates.

Team reference contact

Susana Silva, MSc.