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Regulatory Support

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

  • Management of the review and compilation of the necessary documentation for the submission of CS (e.g. Study Authorization Letter, Investigator’s CV, EC questionnaire, etc.);
  • Reviewing and follow-up of the entire submission process until all required approvals are obtained;
  • Amendments and management of submitted reports 

Please contact us before submitting an CS to obtain the updated list of required documents and templates.



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