Non-interventional studies (NIS) - Dr. Oestreich + Partner GmbH

Non-interventional studies (NIS) compile observations and insights gained during the commercialization phase of approved drugs and certified medical devices. In the area of non-interventional studies (NIS), the primary focus is on data collection and their evaluation with regard to the efficacy, tolerability, economy and application behavior of a product or device. Dr. Oestreich + Partner offers proprietary electronic data capture (EDC) systems for the capture and analysis of the corresponding data that incorporate all legal requirements for non-interventional studies (NIS).

Click here for more information on non-interventional (NIS) studies at Dr. Oestreich + Partner:

Non-interventional studies (NIS)

Customized software for non-interventional studies (NIS)

With regard to increasing demands, statutory requirements and laws, Dr. Oestreich + Partner has developed software solutions that facilitate the needs-based and practical analysis of all data for non-interventional studies (NIS). Our team provides extensive, bundled expertise in both medical and technical fields to enable the creation of our database systems. Our software solutions PMSBOX and OPVERDI are accessible via the Internet to all authorized staff. The OPVERDI documentation system offers numerous options for the display, review and security of the data for non-interventional studies (NIS). With our PMSBOX program, which is also Internet-based, all authorized staff receive current and comprehensive information on the progress of the study at all times and can communicate interactively with each other. Dr. Oestreich + Partner also provides expert consulting services for non-interventional studies (NIS). At our training facilities in Cologne, we regularly provide standardized or customized training for research, marketing and sales staff. Our expert trainers and instructors also provide further education and informational seminars on topics such as non-interventional studies (NIS).

Click here for a general overview of our range of services, including those relating to non-interventional studies (NIS):

Non-interventional studies (NIS)


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

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