Safety in clinical research asks for particular attention.

In cooperation with our project management, acromion GmbH’s medically qualified professionals provide support and assistance to the sponsor's safety surveillance department, as well as to public relations and press department, if requested.

Safety surveillance means:

• development of trial specific safety plans
• training of investigational staff
• SAE-report review for accuracy and completeness
• Preparation of event reports
• CRF safety review
• Reconciliation of SAE data and trial data base