Safety Surveillance


Vigilance in safety surveillance in clinical research asks for particular Attention

In close collaboration with our project management and – if needed – cooperation with a network of long-standing specialized partners, acromion GmbH’s medically qualified professionals provide support and assistance to the sponsor's pharmacovigilance department.

Trust in us for:

  • 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

Your Contact

Dr. Ulrike Schomaker
Project Manager
acromion GmbH

Europaallee 27-29
50226 Frechen

Phone: +49 (0)2234-20 37 37-16
Fax: +49 (0)2234-20 37 37-9


Send us an email