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4-7 - Master Series Program, Part I — Going Paperless: A Smart Way to Increase Site Efficiency and Save Resources
Date/Time:
April 29, 2017 2:30pm - 3:30pm
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5-3 - Master Series Program, Part II — Going Paperless: A Smart Way to Increase Site Efficiency and Save Resources
Date/Time:
April 29, 2017 3:45pm - 4:45pm
Format:
Synced Audio / Video / Slides
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7-3 - Investigator Attrition: Strategies to Turn the Tide
Date/Time:
April 30, 2017 9:50am - 10:50am
Format:
Synced Audio / Video / Slides
7-6 - Regulatory Affairs Committee: 2016 Year-End Review and Looking Ahead
Date/Time:
April 30, 2017 9:50am - 10:50am
Format:
Synced Audio / Video / Slides
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W-2 - Let's Get Clinical! A Clinical Research Boot Camp
Date/Time:
April 28, 2017 8:00am - 5:00pm
10-5 - Maximizing the ROI of Your Clinical Trial Management System
Date/Time:
April 30, 2017 3:45pm - 4:45pm
12-5 - Build a Better Site Budget to Ensure Trial Success
Date/Time:
May 1, 2017 9:45am - 10:45am
Format:
Synced Audio / Video / Slides
18-1 - Optimize Workflow and Resource Allocation Using LEAN-R
Date/Time:
May 2, 2017 11:00am - 12:00pm
Format:
Synced Audio / Video / Slides
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1-3 - Create an Onboarding Curriculum that Fits Your Budget
Date/Time:
April 16, 2016 9:00am - 10:30am
Format:
Synced Audio / Video / Slides
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1-7 - The Immortal Life of Henrietta Lacks: Applying Lessons Learned to Today's Informed Consent Process
Date/Time:
April 16, 2016 9:00am - 10:30am
Format:
Synced Audio / Video / Slides
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2-9 - Rare Disease Research Requires Consciousness, Commitment and Collaboration
Date/Time:
April 16, 2016 2:30pm - 4:30pm
Format:
Synced Audio / Video / Slides
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3-9 - NIH Support of a Single IRB Approach to Review Multicenter Clinical Research and Implications for Academic Centers
Date/Time:
April 17, 2016 8:30am - 10:30am
Format:
Synced Audio / Video / Slides
5-7 - Decoding the New Drug Good Clinical Practice Regulations
Date/Time:
April 17, 2016 4:15pm - 5:15pm
Format:
Synced Audio / Video / Slides
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6-2 - Managing Time, Tasks and Relationships: Focusing on What Matters Most
Date/Time:
April 18, 2016 8:30am - 10:00am
Format:
Synced Audio / Video / Slides
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8-3 - Real-World Study Planning
Date/Time:
April 18, 2016 2:30pm - 3:30pm
Format:
Synced Audio / Video / Slides
8-4 - EU Clinical Trials Regulation: Live in 2016?
Date/Time:
April 18, 2016 2:30pm - 3:30pm
Format:
Synced Audio / Video / Slides
8-7 - An Idea Whose Time Has Come: Next Steps in the Professionalization of Clinical Research
Date/Time:
April 18, 2016 2:30pm - 3:30pm
Format:
Synced Audio / Video / Slides
8-9 - Inside the FDA: Drug Good Clinical Practice Regulations Compliance
Date/Time:
April 18, 2016 2:30pm - 3:30pm
Format:
Synced Audio / Video / Slides
9-7 - Eliminating Shadow Charts from Your Study Site
Date/Time:
April 18, 2016 3:45pm - 4:45pm
Format:
Synced Audio / Video / Slides
10-2 - Building a Better Budget: How Budget Improves Clinical Trials
Date/Time:
April 19, 2016 9:45am - 10:45am
Format:
Synced Audio / Video / Slides
10-9 - Interpreting Clinical Regulations: Precautions and Warnings
Date/Time:
April 19, 2016 9:45am - 10:45am
Format:
Synced Audio / Video / Slides
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11-1 - The Metrics Evolution: Use Better Metrics to Improve Clinical Trials
Date/Time:
April 19, 2016 11:00am - 12:00pm
Format:
Synced Audio / Video / Slides
11-3 - The True Costs of Site Regulatory Compliance and Improvement Opportunities
Date/Time:
April 19, 2016 11:00am - 12:00pm
Format:
Synced Audio / Video / Slides
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S501 - Inefficiencies & Improvement Opportunities in Investigative Site Regulatory Compliance Processes
Date/Time:
April 26, 2015 2:45pm - 3:45pm
Format:
Synced Audio / Video / Slides
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S601 - The Project Manager's Dilemma: Why Am I Too Busy to Manage My Project?
Date/Time:
April 26, 2015 4:00pm - 5:00pm
Format:
Synced Audio / Video / Slides
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S608 - Optimizing Communication Within Global Teams
Date/Time:
April 26, 2015 4:00pm - 5:00pm
Format:
Synced Audio / Video / Slides
S804 - EU Clinical Trials Regulation - Status Quo
Date/Time:
April 27, 2015 9:45am - 10:45am
Format:
Synced Audio / Video / Slides
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S905 - How to Make FDA Inspections as Painless as Possible - What to Expect, What to Do and What Not to Do: A Site's Perspective
Date/Time:
April 27, 2015 11:00am - 12:00pm
Format:
Synced Audio / Video / Slides
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PS408 - Clear the Mud: Current and Future of Cannabis Research
Date/Time:
April 26, 2015 8:30am - 10:30am
Format:
Synced Audio / Video / Slides
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S1007 - Responding to GCP Inspection Findings - Follow-Up and Follow-Through
Date/Time:
April 27, 2015 2:45pm - 3:45pm
Format:
Synced Audio / Video / Slides
S1101 - Hospital-Based Clinical Research Risk Management
Date/Time:
April 27, 2015 4:00pm - 5:00pm
Format:
Synced Audio / Video / Slides
S1102 - Vulnerable Subjects - Do You Know One When You See One?
Date/Time:
April 27, 2015 4:00pm - 5:00pm
Format:
Synced Audio / Video / Slides
S1201 - The Role of Laboratory/ECG Findings in Subject Safety
Date/Time:
April 28, 2015 9:15am - 10:15am
Format:
Synced Audio / Video / Slides
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S1205 - PALM Infrastructure Support Model for Enhanced Knowledge Management for Clinical Teams
Date/Time:
April 28, 2015 9:15am - 10:15am
Format:
Synced Audio / Video / Slides
S1206 - SOPs as Risk-Management Tools: Are Your SOPs Actually Increasing Risk of Non-Compliance?
Date/Time:
April 28, 2015 9:15am - 10:15am
Format:
Synced Audio / Video / Slides
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S1302 - Keeping The Spark Alive During Long-Term, Multi-Center Trials
Date/Time:
April 28, 2015 10:30am - 11:30am
Format:
Synced Audio / Video / Slides
