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 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.
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