It does not work without YOUR input
Before a new medicinal product is introduced to the market, safety, efficacy and tolerability have to be tested. YOU have the experience with your product and we have the experience how to bring YOUR product to YOUR planned market.
Emerging technologies, ever-changing regulations, and increased competition create many challenges for the pharmaceutical and medical product industry. The training courses, developed with government and industry advisors, fulfills a recognized need for comprehensive professional learning in the successful design, development and delivery of medical devices, pharmaceuticals, and other biomedical products. The courses addresses the breadth of the development process, including a thorough understanding of compliance, engineering for improved performance, how to mitigate commercial and financial risks, and building marketing success.
Our training programs are designed to prepare early and experienced stage researchers, academics, physicians, industry and hospital based researchers to conduct, implement and interpret clinical research at the intersection between basic science and clinical medicine. They are designed to bring diverse disciplines together to address the increasing gap between "bench" research and "bedside" application and from bedside application, to improved healthcare quality.
Demonstrating the effectiveness and safety of new medical drugs and products is a critical part of the drug and medical product development process and requires significant resources to accomplish. The program fills a growing need for professional learning that ensures designing and implementing clinical trials for success. The training courses provides comprehensive knowledge of coordinating, monitoring and managing a clinical trial within a framework of good clinical practices and regulatory requirements.