RADI TECH Clinical Trials Management Services (CTMS) incorporate the whole life cycle of Clinical Trials Management and that includes from Concept to realization, implementation and maintenance services offering an end-to-end solution to our clients. The product portfolio includes design, management and implementation of study protocols, the critical building blocks of product development programs. RADI TECH has extensive resources and expertise to design and conduct studies on a global basis, develop integrated global product databases, analyze the data, and prepare and submit regulatory submissions in U.S. Our Clinical Trials Management Services project involves the following components:
  • Protocol and Case Report Form (CRF) design
  • Feasibility study
  • Project management
  • Investigational Site management
  • Investigational Site monitoring
  • Medical monitoring and drug safety
  • Data management
  • Analysis and reporting
  • Medical and scientific publications
  • Regulatory filings

We are strategically positioning our CTMS to be a one stop-over for the clients who are willing to adopt, develop, manage and maintain their Clinical Management. As part of getting industry-wide attention, a great effort is underway by both the teams- Product Development and Management Team to develop it iteratively after the feedback from our clients, has given us greater leverage and advantage over other similar products which were developed in traditional waterfall methodology. Should you have interest in having a demonstration of our greatly appreciated CTMS product, our Sales team is willing to organize and demonstrate the capabilities of CTMS. Please call us or email us with your requirements and our Technical Sales Executives would get in touch with you to discuss and explain how CTMS could help your streamline business.

 

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