Dr. Oestreich + Partner GmbH

Research + Marketing in Medicine + Pharmacy

We are a full-service CRO operating in Europe with certification according to ISO 9001. We offer comprehensive, complete or individual solutions  for clinical studies in the pharmaceutical area (phase II to IV as well as PASS, PAES, NIS, proof of additional benefit, economy studies) for more than 20 years.
We also conduct literature research, perform clinical studies and handle tasks in Regulatory Affairs for Medical Devices with the aim of CE-marking, first registration in the market and keeping your product on the market.

Our customers are:

·         Pharmaceutical companies

·         Manufacturer of Medical Devices

·         Manufacturer of cosmetics

·         Manufacturer of food products

·         Institutions of healthcare

With our in-house EDC-System  (FDA: CFR21 Part 11) we offer since more than 15 years an internet-based user interface and database system, which can be individually configurated for easy, fast and efficient data collection in clinical studies and proves to be a true alternative to paper-CRFs.

Service Overview
- Clinical Investigation
- International Marketing
- Standards
Our mission

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