Patient recruitment - Dr. Oestreich + Partner GmbH

A variety of patient recruitment measures are required depending on the phase of a clinical study. The success and the efficiency of clinical development therefore also depends on reliable and expert patient recruitment. At Dr. Oestreich + Partner GmbH, experienced specialists in a variety of medical fields are available to assist you in all aspects of patient recruitment. With more than 20 years of experience as a full-service contract research organization (CRO), we have a large network of investigator sites that provide cost-effective and flexible implementation of clinical studies with timely patient recruitment. Our staff members also provide competent advisory services for patient recruitment for national as well as international studies.

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Patient recruitment

Structured selection process for patient recruitment

As with all projects we carry out on behalf of companies in the pharmaceutical, biotech, diagnostics, medical technology, cosmetics and nutrition sectors, we focus on customer orientation and rigorous compliance with the highest international standards in patient recruitment. Our services include the drafting and preparation of all required texts, from the documentation for competent authorities and ethics committees to study protocols in accordance with GCP guidelines and templates for investigator contracts as well as statistical analyses and publications. Our customer-oriented service facilitates structured selection processes in accordance with randomization for patient recruitment. Based on various editing systems, suitable patients can be included in order to optimize fast and effective study implementation. The time- and target-sensitive recruitment and monitoring systems play a major role in supporting the investigators and for the steering of the project. Before the start of a study, we provide all staff involved in the investigational site with a detailed, task-based training and qualification to create the prerequisites for a successful project completion.

Click here for an overview of our patient recruitment services:

Patient recruitment

EMA Pharmacovigilance
Health care studies
Observational studies
EMA Pharmacovigilance
Medical Biometrics
Approval of Medical Devices
Clinical Investigators
Clinical Trials
GCP Legislation
GCP - Good Clinical Practice
GCP Guidelines
GCP Compliance
Clinical Research Organisation
Contract Research Organisation
Pharmacoeconomics, Health
Pharmacoeconomic studies
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