The Society of Clinical Research Associates has a full calendar of educational programs slated for March. See below for more details.
(March 6-7 in Dallas, TX)
Objective: This two-day conference is intended to share information among FDA representatives and the regulated community, to facilitate the understanding of regulations, guidelines and practices, and to suggest methods and opportunities to enhance the research professional’s product development experience. The program will focus on the relationships among the FDA and clinical trial staff, investigators and IRBs. The workshop will highlight three areas that present challenges to sponsors and investigational sites: FDA Clinical Research Requirements, Enhancing Success through Communication and Financial Incentives, and Assuring Confidence in Clinical Research.
(March 11-15 in Philadelphia, PA)
Objective: The course contains two modules. 35 hours total CE available. The attendee may elect to attend one (either) or both modules. Module I is the Regulatory / Procedural Module. Module 2 is the Medical / Scientific Module.
(March 14-15 in Philadelphia, PA)
Objective: The goal will be accomplished through lecture, case study, practical application and hands-on experimentation facilitated by experienced clinical research professionals. Information and practical application recommendations will be discussed regarding all of the functions of the research site related to finance, productivity, budgeting, billing, and executive reporting.
(March 21-22 in Las Vegas, NV)
Objective: The goal will be accomplished through lecture, case study and practical application facilitated by clinical research professionals. Information and practical application recommendations will be presented and discussed regarding Clinical Trial Management Systems, CTMS evaluation, selection, implementation and management.