Dr Oestreich und Partner:

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.


Clinical trials, Product marketing, Medical writing, Regulatory Affairs






© 2015 The World of CROs. All rights reserved.