Clinical development - Dr. Oestreich + Partner GmbH

The CRO team at Dr. Oestreich + Partner has been providing an extensive range of clinical development services for over 20 years. Our outstandingly qualified staff provide our clients with customized, practical solutions for the multidisciplinary requirements and fields of clinical development at both national and international levels. We carry out all investigation for our clients and procure all of the documentation necessary for the generation of protocols and trial plans as well as investigator templates and reports. Upon request, we also establish the necessary contacts with all institutions and competent authorities required and accompany our clients to meetings. We also arrange licensing, editing of medical and scientific informational publications and postal and electronic mailings. From the initial planning to the successful completion of clinical development, we remain in constant contact with our clients every step of the way and provide expert, goal-oriented instruction for everyone involved in the project.

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Clinical development

Clinical development with customized documentation systems

As a “pioneer” in Germany we provide particularly efficient software to our clients for the recording and evaluation of the extensive data in all phases of clinical development for over 10 years. The Internet-based documentation systems OPVERDI and PMSBOX enable the creation of customized, multilingual electronic case report forms (eCRFs) as well as the import of external data, e.g. from imaging procedures, laboratories or telemedical monitoring systems. All authorized staff members involved in clinical development are networked via our software solutions, saving time and money and enabling interactive communication. Investigators, project managers, monitors, data managers and all other authorized users of clinical study data can review, edit and update the data within the limits of their respective access rights and permissions.

Click here to find out more about our clinical development services:

Clinical development


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