"Multinational implementation helps prevent problems"

Our customised services help investigators  streamline the process of patient screening, recruitment, and enrollment. Different powerful site management tools are available so as to involve the right patients more quickly and to improve study start-up. Our time-sensitive recruitment steering tools and our controlling systems are essential instruments  in supporting  the investigator and in accelerating the  development of the clinical trials. 

Before even starting a clinical trial at an investigator´ s site we ensure that those invoved are qualified enough to carry out the study.  If all specific clinical trial criteria is met, they will go through a rigorous screening and selection process.


Clinical Trial Management
(e)CRF-Development
Patient Recruitment
On-site/Off-site Monitoring
Economic Studies
Biometrics
Budget Management
Product Safety
Medical Writing
Our experience ...

EMEA Pharmacovigilance · Health care studies · Observational studies · EMA Pharmacovigilance · Medical Biometrics · Approval of Medical Devices · Pharmacovigilance · Clinical Investigators · Clinical Trials · GCP Legislation · GCP - Good Clinical Practice · ICH GCP E6 · GCP Guidelines · GCP Compliance · BfArM GCP · CRO – Clinical Research Organisation · CRO – Contract Research Organisation · PSUR · PSURs · Pharmacoeconomics, Health · Pharmacoeconomic studies · Pharmacoeconomics · Patient Monitoring · Monitoring Clinical Trials · Clinical Monitor · Marketing Authorisation · Medicinal Product Approval · Drug safety · Data management plan · Clinical development · Monitoring investigators · Non-interventional studies (NIS) · Patient recruitment · Phase IV studies · Investigator audit · Investigator qualification · Investigator selection