We follow the guidelines of our Quality Management System (QMS) in all activities we develop.
The QMS aims to maintain the quality standards in the conduction of clinical trials, conforming with the requirements established by national and international regulations in clinical trials: Good Clinical Practice (GCP), Document of the Americas, Declaration of Helsinki, Resolution 466/12, IN ANVISA 04/09.
The QMS is described in the Quality Manual.
In addition to the quality politics of CBED, this document describes the Standard Operating Procedures (SOPs), the respective forms and records, and it establishes corrective, preventive and improvement actions.
Our QMS is reviewed annualy or earlier, if an update is ugently required.
