Investigator qualification - Dr. Oestreich + Partner GmbH

The guidelines of good clinical practice (GCP) and the German Drug Law (Arzneimittelgesetz, AMG) require a special investigator qualification. An investigators must be familiar with the special features of clinical studies and is responsible for consulting, treating and supporting patients who participate in a clinical trial. The investigator ensures the compliance with statutory regulations and clinical research requirements. Knowledge of project management and ethical requirements as well as methodological and practical expertise is of key importance with regard to the qualification as investigator. The qualification as an investigator also requires a briefing on quality assurance measures, the efficient use of electronic media and the targeted evaluation of the data collected.

Click here for more information on the qualification as an investigator at Dr. Oestreich + Partner:

Investigator qualification

Informational events and training courses for investigator qualification

In the area of clinical research, our experienced team of specialists also supports you in the qualification of investigators. Our staff acquired its expertise over many years of work in medical facilities, scientific and academic institutions or international corporations, and places their combined expertise on medical and technical issues at the disposal of our clients and investigators for clinical research projects. Thanks to our extensive international network, we can provide flexible assistance in an extremely wide range of medical fields and can refer to our longstanding experience in the qualification of investigators for clinical projects at both the national and international level. At our training facilities in Cologne, we regularly provide standardized and customized training for research, marketing and sales staff. Our expert trainers and instructors also provide further education and informational seminars on the qualification of investigators.

Click here for comprehensive information on our services in clinical research and investigator qualification:

Investigator qualification


EMA 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
Clinical Research Organisation
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

EMA 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 · Clinical Research Organisation · 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