| Next Workshop: September 13-14, 2010 Chicago (Oak Brook) IL This workshop brings to life FDA and ICH guidelines for conducting clinical trials by covering a trial from the site perspective in sequence, from pre-study visit to study closeout. The course is designed for new study coordinators (CRCs), research nurses or clinical trial investigators and for any site professional without formal GCP training. Learn more >
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| Next Workshop: October 25-26, 2010 Dallas TX Last 2010 Session! This workshop covers clinical trial management beyond routine coordinating. Topics include basic clinical trial budgeting, medical device regulations, clinical trial protocol analysis, FDA audits, ethical issues and site team communications. This class is targeted at experienced study coordinators (CRCs), research nurses, clinical trial investigators and clinical research site professionals who have attended basic training in clinical trial coordination and/or who have equivalent knowledge of FDA guidelines and GCPs. Learn more >
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| Next Workshop: September 27-28, 2010 Philadelphia PA
This workshop covers clinical trial finances from using financial protocol analysis to build a trial budget to tracking financial activity and working with financial reports. This class is for experienced clinical research nurses, study coordinators (CRCs), investigators, research administrators or any clinical team member with a fiscal responsibility. Attendees should have attended basic training in clinical trial coordination and/or have equivalent knowledge of FDA regulations and GCPs. Learn more >
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