"Sooner or later – the risk/benefit ratio determines a product’s future"

Upon request we can arrange drug/product packaging, labelling, storage and 'to site' shipment. We prepare randomisation coding, telephone randomisaton and emergency envelopes as well as supplying a 24 hour hotline for emergency decoding and adverse event reporting.

We supply tele-monitoring tools for patient self monitoring to observe the compliance, efficacy and safety of treatment activities.


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