MEDICRO is an independent high-class full-service CRO with its office in Nuremberg. MEDICRO has been a member of the Federal Association of Contract Research Organisations (Bundesverband Medizinischer Auftragsinstitute (BVMA)) since 2009. In accordance with their Articles of Association a system audit was carried out successfully. Having been admitted to the BVMA, MEDICRO is regularly audited for quality assurance by an external independent organization appointed by the Association. This measure guarantees continued high quality standards.
Our years of experience in clinical studies (Phase I – IV) in different therapeutic areas form the basis for the successful scientific conduct of clinical trials.
Due to our extensive experience we can assure you that the requirements of our clients in the pharmaceutical sector are met in a cost-effective and targeted manner. Our scientific approach guarantees first-class quality when it comes to conducting clinical trials.
It is our goal to offer our clients top quality services.
Working with a small, efficient and highly motivated team at MEDICRO, we can afford to be flexible and adapt to your wishes quickly while still offering solutions without bureaucracy. This saves both time and costs – your costs, to be exact. Our strengths are flat hierarchical structures, a high level of personal responsibility as well as expertise.
We offer all study related services from one source - study design, data management, project management, clinical trial monitoring, statistical data analysis and, if requested, all translations of your study documents into German or into English. Thus we can ensure that your clinical trial is brought to a successful conclusion in a quick and cost-effective manner.
Medicro - http://www.medicro.de