DRC is specialized in assisting companies from market access strategy over clinical development strategy to the full setup and management of clinical trials. In parallel we offer clinical quality services ranging from audit services to the full development or optimization of quality management systems.
Our mission is adding value through a customized approach ensuring success from the very beginning in clinical research. As no two clinical development paths are ever the same, we at DRC, strongly believe in partnering with our client as of the transition from pre-clinical to clinical research. This minimizes the risk of late-stage development failures, increases the probability that optimal safety and efficacy data are available and decreases the total time involved with drug or medical device development.
Our high-quality standards and continuous investment in e-solutions, staff and training, ensures delivery within the expected timelines and an all-time inspection readiness. Our personal approach is key in our believe that we are not just a service provider but a trusted partner for the long-run.
• Optimization of TPP / Market Access Strategy
• Clinical development strategy & Project Management
• Regulatory strategy
• Protocol/study optimization
• Study Feasibility
• Project Management
• Monitoring Services
• Patient recruitment
• Data Management & Statistics
• Medical Writing
• Warehousing and Distribution
• Lab services
• Conducting sponsor and investigational site audits
• Vendor assessments
• Developing or optimizing Quality Management Systems