Since 1993 ClintraQ is active as a CRO for the pharmaceutical industry.
Based on the multidisciplinary experience of the personnel, ClintraQ GmbH is able to provide a wide spectrum of services. After studying biology and a Ph.D. in endocrinology or toxicology, respectively, we collected practical experience in several areas of drug development, as such: pre-clinical work in compliance with GLP, clinical studies of phase I to IV according to GCP, Quality Management in GMP, ISO 9001:2000 and ISO 13485:2003 as well as regulatory affairs.
Different mother tongues, the ability to speak different languages and the technical knowledge in various disciplines of natural sciences, provide the ideal background for the translation of scientific and medical texts.
In Switzerland, Italy, Germany, France or England monitoring or audits are performed in the local language improving the mutual understanding and avoiding communication problems.
Continuous education and co-operation with different companies allow us to keep up-dated and to adapt our services to the respective necessities.