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.
Established in 1985, medicomp offers a wide range of services in drug and medical device development throughout Europe, from early conception of a study to the final report.
mdt medical device testing GmbH supports medical device manufacturers to reach their objectives of developing, producing and marketing medical devices of superior quality.
LKF - Laboratorium für Klinische Forschung GmbH – was established in 1991. The founder, Prof. Dr. W. Junge, M.D., after experience of clinical trials in his medical routine laboratory, recognized the necessity and advantage of forming a separate and specialized medical laboratory unit dedicated exclusively to supporting clinical trials of phases I – IV. Today, LKF has more than 70 employees and is owned by four partners of different medical backgrounds. LKF has set up a stringent quality management system based on the international guidelines GCP and ISO 17025.
INTERLAB is a leading provider of regional, international and global central laboratory services for clinical trials run by pharmaceutical and biotech companies. INTERLAB fosters the development of our staff and performs all services to the highest quality and ethical standards.
Health Research Services (HRS) GmbH is an independent contract research organisation offering specialist services in the areas of Consulting, Scientific Drug Research & Development, Project Management, Clinical Monitoring, Medical Writing and Regulatory Affairs.
FGK Clinical Research GmbH is a full service contract research organization offering a complete range of clinical development and consulting services to pharmaceutical, biotechnology and medical device companies.
With more than 70 highly skilled and experienced people, FGK operates out of Munich on local and global projects, covering clinical studies from phases I to IV. FGK has extensive experience in all major therapeutic areas and clinical research fields, which allows it to effectively design, manage and analyze your development programs and clinical trials.
emovis was founded in 2001 by several physicians, that had already made experiences in various sectors of clinical research. The company is headquartered in West-Berlin, near Kurfürstendamm. They position them as specialized test center. This means that they treat their patients in phase II-IV studies.
Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab.
Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India.
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: