A German SME, full-service CRO, offers a broad range of professional services and partner solutions for international small and mid-sized pharmaceutical, biotech and medical device companies.
Their service include planning of studies, preparation of study protocols, monitoring, design and implementation of case report forms (CRFs). They are also experienced in regulatory affairs e.g. applications for ethical votes and permissions.
Furthermore the CRO offers recruitment, assessment and initiation of study centres and training of investigators and their staff. They monitor study centres, check CRFs for completeness, plausibility and safety including source data check. The German company maintains the communication between investigators / sponsor, supplies study centres with documentation, transfers study data and does all the reporting.
In more than 30 years the German SME has created a network of motivated specialists in Germany and the rest of Europe. Moreover, they further expanded their services in collaboration with specialised partners in the U.S. and India/Asia. In each of these countries they have local monitors who are supervised by experienced colleagues. They can offer a wide range of medical specialists.
The previous conducted studies have been realised for well-known large pharma companies.
The CRO wishes to collaborate with small and medium-sized companies as well.
The company is looking for industrial/ academic partners in the field of clinical trials for service agreements / subcontracting.
Also sponsors (investors) with an interest in planning and conducting a clinical trial
are sought. This applies to companies and academic institutions in the pharma or biotech sector.