Buero Neumann was founded by Jutta Neumann on 01 July 1998. Before this time Jutta was working as GP in Germany after studying medicine in Germany (Aachen) and Belgium (Antwerp).The Freelance Office is located at the border area of Germany, Belgium and The Netherlands.
Buero Neumann supports pharmaceutical Clients, CROs and Investigators in a wide range of indications and study designs and meets high quality standards in fulfilling your project’s needs. The Clinical Service is provided with help of a firm employed CTA and a CRA colleague (also freelancer).
We offer you professional support from the very beginning of your Clinical trial in all Phases (Phase I-IV) to study end.
All activities are carried out according to the national and international laws and guidelines (AMG (German Drug Law), GCP/ICH, and/or FDA, CFR) and in accordance to the Standard Operating Procedures of the client.
Our focus is on non-German small to medium size clients being a CRO or a biotech or pharmaceutical company. We work together with a team of hand selected CRA and PM colleagues. We do not subcontract! We are not a CRO! We can provide the full CRO Service though if needed with help of dedicated PMs who have all more than 20 years of experience in the conduct of clinical trials and are all well linked up with other Service Providers for Clinical trials.