Our broad therapeutic experience, strong project management capabilities, and core expertise in quality assurance and regulatory affairs enables us to address specific product development needs and mitigate obstacles often present in pharmaceutical and medical device development.
Clinartis provides comprehensive study monitoring and site management services. Our skilled and well-trained monitors support the entire study life cycle from investigator selection through database closure and ensure the highest quality review of data and effective interaction with study sites.Read More
Clinical research project requires a broad range of skills and expertise in various disciplines in order to plan, administer, track, evaluate and report activities. Our project management team members with a variety of backgrounds have vast experience in managing clinical studies, anywhere from first-in-man trials to multi-country Phase III studies.Read More
Clinical Data Management is one of the main elements of our services portfolio. As part of our data management services we offer traditional paper-based CRFs, EDC systems as well as data integration with other data systems such as central laboratories, central readers, IVRS, etc. Using thoughtful review process we recommend the most efficient, cost-effective data capture technologies to ensure high-quality, accurate, reliable, and statistically sound data from clinical studies.Read More
Our highly experienced clinical research physician network provides medical support and training to study team and assure the complete, consistent and timely assessment and documentation of adverse events.Read More
Clinartis provides a full range of independent GCP audit capabilities and quality assurance support. We developed proven systems approach methodologies for the conduct of audits at investigator site, clinical research organizations, data management and analysis, central reading facilities, central laboratory facilities, software systems and drug supply management vendors.Read More
Clinartis has dedicated resources which enable us to provide regulatory solutions to support your product development programs. We provide comprehensive regulatory services across the spectrum of global product development, registration and commercialization.Read More