31st Annual Meeting (2010)

Baltimore, Maryland, USA

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SCT Business Session Minutes »

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Videos:

		SCT President Welcome		Colin Begg	00:07:04
		Presentation of the Class of 2010 Fellows			00:20:58
		Curtis Meinert Lecture: "FDA, Clinical Trials, and Public Health"		Joshua Sharfstein	00:33:01
		Founders Lecture: "Publicly Funded Clinical Trials in the Era of Comparative Research Effectiveness"		Richard Schilsky	00:48:38
		WORKSHOP P7: Adaptive Clinical Trials
			P7-Part 1: Short Course: Adaptive Clinical Trials	Roger Lewis	00:44:53
			P7-Part 2: Adaptive Dose-Ranging Designs and Methods	José Pinheiro	00:44:25
			P7-Part 3: Bayesian Adaptive Designs for Clinical Trials	Jason Connor	00:44:41

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Slides from 2010 Meeting Presentations:

Trial of the Year, SACKETT-IMPACT
Sackett-ImpACT-MRC TB-Streptomycin - Baltimore 2010.pdf


Workshops:

• Workshop P1 - Essentials of Randomized Clinical Trials
• Workshop P2 - Bayesian Methods
• Workshop P3 - Design and Interim Data Analysis of Clinical Trials
• Workshop P4 - The Role of Standards: Vocabulary and Data Elements to Support Clinical Trials
• Workshop P5 - Trial and Site Management for Multi-Center Trials
• Workshop P7 - Adaptive Clinical Trials
• Workshop P8 - Design and Anaylsis of Gene Expresssion Data
• Workshop P9 - Essentials of Clinical Data Management
• Workshop P10 - Considerations in the Design of Clinical Trials for Comparative Effectiveness
• Workshop P11 - I am NOT a Statistician but I understand what you are saying

Invited Sessions:

• Invited Session 3 - Overcoming Challenges in Information Integration
• Invited Session 6 - Global Harmonization of Clinical Trials (1)
• Invited Session 6 - Global Harmonization of Clinical Trials (2)

Contributed Paper Sessions:

• CPS Session 1A - Trial Conduct - Long-term follow up of clinical trials: is it worth it? Allan Hackshaw, University College London
• CPS Session 1B - Trial Management and Efficiency (1) -Speed to Market: A Nutrition Industry's Experience in Streamlining the Pediatric Clinical Research Process; Geraldine Baggs, Abbott Nutrition, Abbott Laboratories
• CPS Session 1B - Trial Management and Efficiency (2) - Enabling Efficient Electronic Regulatory Submissions for Medical Devices Using CDISC Data Standards; Kit Howard, Kestrel Consultants, Inc.  
• CPS Session 1C - Statistical Issues (1) - The Effect of an Unplanned Sample Size Re-Estimation on the Type I Error Rate - Leslie McClure, University of Alabama at Birmingham
• CPS Session 1C - Statistical Issues (2) - Exploratory Graphical Summaries of Longitudinal Concomitant Medication Data - Chris Barker, Consultant
• CPS Session 1C - Statistical Issues (3) - Power in Three-Arm Generic Drug Trials of Equivalence - Young Kim
• CPS Session 1D - Data Management (1) - Case Report Form Design for Web-based Clinical Trial Data Management Systems - Catherine Dillon, Medical University of South Carolina
• CPS Session 1D - Data Management (2) - E-PROJECT:  A WEB-BASED SYSTEM TO ENHANCE THE PURE MATRIX OF PROJECT MANAGEMENT FOR BIOSTATISTICAL INFORMATICS- Megan Parks, University of Kansas Medical Center
• CPS Session 2C - Trial Closeout and Web-Based Trial Management -- Ending a Clinical Trial with Clean Data -- It's Achievable
• CPS Session 3A - Statistical Issues - DESIGN CHALLENGES FOR CLUSTER RANDOMISED TRIALS IN STROKE REHABILITATION - Ivana Holloway, University of Leeds
• CPS Session 4C - Ethical Issues - An Approach for the Total Amendment of "Ethical Guidelines for Clinical Studies" in Japan -Development of a Systematic Educational Program-; Toshinori Murayama, Kyoto University Hospital
• CPS Session 4E - Survivial Analysiss - The Analysis of Case Cohort Design in the Presence of Competing Risks with Application to the Analysis of the Effect of Treatment for Hodgkin Lymphoma on Cardiac Events; Melania Pintilie, Ontario Cancer Institute