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Preconference Tutorial
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Trk 01: Clinical Operations
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Trk 02: Proj-Port Mgt-Strat Planning
All
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Trk 02: Proj/Port Mgt/Strat Planning
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Trk 03: Innov Part Model-Outsourcing
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Trk 03: Innov Part Model/Outsourcing
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Trk 04: Preclin Transl-Early Clin Dev
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Trk 05: Reg of Prod Adv-Mkting
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Trk 07: Tech-Data- Records-Subs
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Trk 07: Tech/Data/ Records/Subs
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Trk 09: Med Devices-InVitro-CombProd
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Trk 09: Med Devices/InVitro/CombProd
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Trk 10: Pub Pol-HealthCare Compl-Law
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Trk 10: Pub Pol/HealthCare Compl/Law
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Trk 11: Quality in CT-GCP
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Trk 11: Quality in CT/GCP
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Trk 12: Pharm Quality
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Trk 13: CER-Glob Health Econ
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Trk 13: CER/Glob Health Econ
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Trk 14: Clin Safety-PV
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Trk 14: Clin Safety/PV
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Trk 15: Statistics
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Trk 16: Prof Development
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Trk 17: Rare-Orphan Diseases
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Trk 17: Rare/Orphan Diseases
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Trk 18: Global Regulatory
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Trk 19: DIAmond
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Trk 20: Innov Theater
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Trk 21: Poster Presentations
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Trk 22: Engage and Exchange
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Credit Type
ACPE
CME
IACET
PMI
RN
Audience
Advanced
Basic
Intermediate
Featured Topics
21st Century Cures
Agency Participation
Approval Pathways
Audits and Inspections
Benefit-Risk
Big Data
Biologics-Biosimilars
Clinical Trial Designs
Clinical Trial Transparency-Clinical Trial Disclos
Cloud Computing
Community-led-Scientific Working Group Offerings
Current Issues in Policy and Law
Design Thinking
Disease Specific
Disruptive Technologies
Electronic Health Records (EHR)
Emerging Markets
GDUFA-Generics
Hot Topics in Policy and Law
IDMP
Increasing Research and Development Innovation
Interactive Workshop
Labeling
Mobile-Wearable Technology
Observational Studies
Partnership Strategies
Patient Engagement
Patient Recruitment and Retention
Patient Registries
Pediatrics
Precision-Personalized Medicine-Targeted Therapy
Pricing- Reimbursement and Access
Program Offerings for Student Attendees
R&D Innovation
Regulatory Harmonization-Convergence
Risk Evaluation and Mitigation Strategies (REMS)
Risk-Based Monitoring
Social Media Strategies
Topics Related to Asia-Pacific Region
Topics Related to Canada
Topics Related to China
Topics Related to Europe-EMEA
Topics Related to India
Topics Related to Japan
Vaccines
Value-Based Evidence
Women's Health
Interest Area
Academic Health Centers-Investigative Sites
Advertising & Promotion
Biotechnology
Clinical Data Management
Clinical Data Management - eClinical
Clinical Research
Clinical Safety & Pharmacovigilance
Clinical Supplies
CMC
CMC-GMP
Combination Products
Comparative Effectiveness
Document & Records Management
eClinical
Finance
Good Clinical Practices & QA
Information Technology
Manufacturing
Marketing & Sales
Medical Communications
Medical Devices & Diagnostics
Medical Science Liaison
Medical Writing
Non-clinical Safety
Outsourcing
Patient Engagement
Pharmaceutics
Pricing - Reimbursement
Professional Education - Training & Development
Project Management
Public Policy - Health Care Compliance - Law
Public Policy - Law
QA-QC
Quality Assurance - Quality Control
R&D - Strategic Issues
Rare - Orphan Diseases
Regulatory Affairs
Statistics
Strategic Planning
Study Endpoints
Submissions
Val - Electronic Info Integrity
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Sunday
, June 26
8:30am EDT
#24: Regulatory Considerations for Drug and Medical Device Development: Current Status and Trend of IND/NDA Practices in China
104AB
#23: How to Prepare for an FDA Inspection
103A
#25: Signal Detection: Identifying and Managing Safety Signals
105AB
9:00am EDT
#40: Analysis of Safety Data from Clinical Trials
111AB
#42: Clinical Statistics for Nonstatisticians
113A
#41: A Rare Disease Program Case Study: Strategies for Successful Outcomes
112AB
1:00pm EDT
#31: Preparing for a US FDA Advisory Committee Meeting
103A
#34: Ethical Issues in Clinical Trials
104AB
#33: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports
107AB
#37: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model
108A
Monday
, June 27
8:30am EDT
#106: Fostering a Partnership to Advance Innovation: Niche Service Leads to Breakthrough in Patient Recruitment and Retention Challenges
112AB
#101: Opportunities for Improving Informed Consent of Clinical Research Volunteers
113C
#102: Digital Health Debate
113A
#103: Decision Tools to Drive Efficient Recruitment and Retention: Making Recruitment a Science
113B
#107: Fatal Drug Trials in Phase 1: Understanding Risk, Subject Safety, Timelines, and Cost
202AB
#113: Clinical Developments in Immuno-Oncology, Part 1 of 2: Science, Current Methodologies, and Achievements
108B
#112: The Upcoming European Clinical Trials Regulation
204C
#114: Bringing the Trial to the Patient: Making the Patient Voice Central from Trial Design Onward
204A
#119: Narrative Medicine: Innovative Techniques for Including the Voice of the Patient in Clinical Trials
102AB
#121: Rare Disease Clinical Trials: Coping with Unique Challenges
103A
10:00am EDT
#122: DBMS Consulting/Clinical Ink Innovation Theater: Accelerating Clinical Trial Innovation: Technology Case Studies for Improving Data Collection, Monitoring, and Medical Coding Processes
Exhibit Hall B
10:45am EDT
#123: Global Clinical Trials: Innovative Approaches to Clinical Trials in Japan, India, and Latin America
113B
#124: Risk-Based Monitoring in Clinical Trials
113C
#125: Patient Recruitment in Rare Diseases: Ideas and Framework for Out-of-the-Box Exploration
113A
#126: Hope Is Not a Strategy: Quantifying Knowledge for Better Decision Making in Clinical Development
102AB
#130: Take Two Aspirin and Text Me in the Morning: Technology Suited for 20,000 Virtual Patients on the PCORI Aspirin Trial
201C
#133: Take Advantage of Global Expedited Pathways: Breakthrough, Sakigake, PRIME!
201B
#135: Clinical Developments in Immuno-Oncology, Part 2 of 2: Clinical Implementation of Biomarkers
108B
#136: Clinical Data Disclosure and Transparency: ClinicalTrials.gov Final Rule, EU Requirements, and Other Key Updates
202AB
#137: Using Technology to Make Trials Accessible to More Clinical Trial Participants
204A
1:45pm EDT
#150: Quintiles Innovation Theater: Evidence Optimization: Fueling Smarter Clinical Development and Value Generation
Exhibit Hall B
4:30pm EDT
#153: BBK Innovation Theater: Reimagining the Patient Experience Through mHealth Technologies
Exhibit Hall B
Tuesday
, June 28
8:00am EDT
#202: Changing Cultures to Advance Patient Engagement
103ABC
9:45am EDT
#206: Covance Innovation Theater: Leveraging Patient Data and Historical Investigator Performance Data to Realize Faster Patient Recruitment
Exhibit Hall B
10:30am EDT
#207: Advancing the Appropriate Use of Mobile Clinical Trials: The Clinical Trials Transformation Initiative
108A
#222: Valuing the Clinical Trial Patient
204A
#224: Identifying Patient-Centered Outcomes for Use in Observational Research: Why and How
201A
#208: Measuring Return on Engagement: An Interim Report on the DIA-Tufts CSDD Metrics Study
108B
10:45am EDT
#228: Increase Value of Clinical Trials Through Impactful Branding
Exhibit Hall A
12:00pm EDT
#230: Quintiles Innovation Theater: Transforming Patient Recruitment Through Site and Patient Engagement
Exhibit Hall B
2:00pm EDT
#235: Global Clinical Supply Logistics Study
113A
#234: TransCelerate's Risk-Based Monitoring: Sharing What We Are Learning
109AB
#240: CFAST at Year Three: Innovative Approaches to Adding Breadth, Depth, and Value to Therapeutic Area Standards
204B
#250: Open-Label, Long-Term Extension Studies: Study Designs and Ethics
201A
4:00pm EDT
#278: Real Life Application of Risk-Based Monitoring
Exhibit Hall A
#257: Mobile Apps for Clinical Trials: DIY or AMAZON Strategy? When to Build, When to Buy
113A
#260: A Risk-Benefit Approach to Planning Early Clinical Development
113C
#263: Patient Centricity in Clinical Trials
201B
#265: Enabling Innovative New Endpoint Measurement Using Mobile Technology
203AB
#271: The Things Kids Say: Clinical Outcome Assessments in Pediatric Clinical Trials
103A
#276: Using Input from Patient Communities to Develop PRO Instruments
103C
Wednesday
, June 29
10:30am EDT
#314: Transforming Clinical Protocols into a Digital Platform: Driving Quality and Efficiency End-to-End
203AB
#318: Changes to Common Rule Likely Affecting FDA-Governed Research
202AB
#307: Mythbusting Site Productivity: Referral Practices and Untapped Site Options
108A
#308: Patient Recruitment Workshop: Survey Results and Practical Application
102AB
#313: The Future of Clinical Research Data: 2020 and Beyond
204B
#315: Enhancing Pediatric Product Development in a Global Regulatory Environment: Extrapolation and Modeling and Simulation, Oh My!
201B
#316: What’s Your Preference? The Emerging Importance of Patient Preference Elicitation
204C
#319: Unlocking the Mysteries of Knowledge Management and Potential Applications for Clinical Development
204A
#324: Implementing Adaptive Designs Involves Greater Teamwork
109AB
12:00pm EDT
#330: SAS Innovation Theater: Empowering Action – Fueling Safety and Operational Efficiency
Exhibit Hall B
2:00pm EDT
#341: eTMF: Selection, Implementation, and What's Next?
204B
#351: Emergent Study Designs and Analysis Methods Addressing Issues Associated with Pediatric Clinical Studies
108B
#353: The Utility of Natural History Studies in Drug Development and Approval
103C
#354: Protocol Optimization: Making It Real
Exhibit Hall A
#334: Risky Business: Latest Trends, Strategies, and Tools for Predicting Success and Monitoring Risk During Clinical Trial Operations
113B
#335: Multi-Ethnic, Special Populations, and Patient Diversity in Clinical Trials
113C
#338: Evolving Methods in Pain Trials: Evaluating Abuse Deterrence, Drug Interactions, and Appropriate Patient Selection
201A
#342: Big Data in Health Care and Life Sciences
201C
#340: eSource: Using Source Data Capture from Electronic Health Records to Improve Clinical Research
204C
#346: Anticipating and Responding to Challenges in Issue Management
204A
4:00pm EDT
#360: Biomarkers and Sample Stability: Bottlenecks in Study Planning, Ensuring Sample Stability as the Key for Reliable Lab Results
105AB
#361: Protocol Endpoints: A Clear Map to Navigate the Yellow Brick Road and the End of Endpoint-Creep
203AB
#367: Quality at the Edge(s): Design It Right and Keep It Going in Non-Interventional Studies
204A
#371: FDA and PatientsLikeMe: Exploring the Use of Patient-Generated Data in Drug Safety
113A
#357: The Internet of Things and Clinical Research: Privacy, Security, and Ethical Aspects
108B
#366: Infectious Disease Containment and Lessons Learned
202AB
#373: Safety Reporting Pitfalls and Successes for Oncology and Hematology Drugs
113B
#376: Pediatric Rare Disease Drug Development
103C
Thursday
, June 30
9:00am EDT
#402: Protocol Development Is a Team Sport
103ABC
10:45am EDT
#407: Successful Application of Wearables and Remote Monitoring in Clinical Trials: Lessons Learned and Future Progress
111AB
#403: Running Personalized Medicine Trials: Facts and Figures
108B
#406: Navigating Partnerships and Submissions: Best Practices for Successful Medical Writing Deliverables Involving Multiple Stakeholders
113A
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DIA 2016 Annual Meeting
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DIA 2016 Annual Meeting
Jun 25
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CME
IACET
PMI
RN
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Advanced
Basic
Intermediate
Featured Topics
21st Century Cures
Agency Participation
Approval Pathways
Audits and Inspections
Benefit-Risk
Big Data
Biologics-Biosimilars
Clinical Trial Designs
Clinical Trial Transparency-Clinical Trial Disclos
Cloud Computing
Community-led-Scientific Working Group Offerings
Current Issues in Policy and Law
Design Thinking
Disease Specific
Disruptive Technologies
Electronic Health Records (EHR)
Emerging Markets
GDUFA-Generics
Hot Topics in Policy and Law
IDMP
Increasing Research and Development Innovation
Interactive Workshop
Labeling
Mobile-Wearable Technology
Observational Studies
Partnership Strategies
Patient Engagement
Patient Recruitment and Retention
Patient Registries
Pediatrics
Precision-Personalized Medicine-Targeted Therapy
Pricing- Reimbursement and Access
Program Offerings for Student Attendees
R&D Innovation
Regulatory Harmonization-Convergence
Risk Evaluation and Mitigation Strategies (REMS)
Risk-Based Monitoring
Social Media Strategies
Topics Related to Asia-Pacific Region
Topics Related to Canada
Topics Related to China
Topics Related to Europe-EMEA
Topics Related to India
Topics Related to Japan
Vaccines
Value-Based Evidence
Women's Health
Interest Area
Academic Health Centers-Investigative Sites
Advertising & Promotion
Biotechnology
Clinical Data Management
Clinical Data Management - eClinical
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Clinical Safety & Pharmacovigilance
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CMC-GMP
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Comparative Effectiveness
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Medical Science Liaison
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Outsourcing
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Professional Education - Training & Development
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Public Policy - Health Care Compliance - Law
Public Policy - Law
QA-QC
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Val - Electronic Info Integrity
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Saturday
, June 25
Sunday
, June 26
Monday
, June 27
Tuesday
, June 28
Wednesday
, June 29
Thursday
, June 30
Venue
102AB
103A
103ABC
103C
104A
104AB
105AB
107AB
108A
108B
109AB
111AB
112AB
113A
113B
113C
114
201A
201B
201C
202AB
203AB
204A
204B
204C
Ballroom A
Ballroom AB
Exhibit Hall
Exhibit Hall A
Exhibit Hall B
Liberty Ballroom A
TBA
TBD
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Preconference Tutorial
All
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Trk 01: Clinical Operations
All
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All
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Trk 04: Preclin Transl-Early Clin Dev
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Trk 05: Reg of Prod Adv-Mkting
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Trk 11: Quality in CT/GCP
All
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Trk 12: Pharm Quality
All
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Trk 13: CER-Glob Health Econ
All
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Trk 13: CER/Glob Health Econ
All
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Trk 14: Clin Safety-PV
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Trk 14: Clin Safety/PV
All
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Trk 15: Statistics
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Trk 16: Prof Development
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Trk 20: Innov Theater
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Trk 22: Engage and Exchange
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Trk 23: Opening Plenary
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Other Filters
Credit Type
ACPE
CME
IACET
PMI
RN
Audience
Advanced
Basic
Intermediate
Featured Topics
21st Century Cures
Agency Participation
Approval Pathways
Audits and Inspections
Benefit-Risk
Big Data
Biologics-Biosimilars
Clinical Trial Designs
Clinical Trial Transparency-Clinical Trial Disclos
Cloud Computing
Community-led-Scientific Working Group Offerings
Current Issues in Policy and Law
Design Thinking
Disease Specific
Disruptive Technologies
Electronic Health Records (EHR)
Emerging Markets
GDUFA-Generics
Hot Topics in Policy and Law
IDMP
Increasing Research and Development Innovation
Interactive Workshop
Labeling
Mobile-Wearable Technology
Observational Studies
Partnership Strategies
Patient Engagement
Patient Recruitment and Retention
Patient Registries
Pediatrics
Precision-Personalized Medicine-Targeted Therapy
Pricing- Reimbursement and Access
Program Offerings for Student Attendees
R&D Innovation
Regulatory Harmonization-Convergence
Risk Evaluation and Mitigation Strategies (REMS)
Risk-Based Monitoring
Social Media Strategies
Topics Related to Asia-Pacific Region
Topics Related to Canada
Topics Related to China
Topics Related to Europe-EMEA
Topics Related to India
Topics Related to Japan
Vaccines
Value-Based Evidence
Women's Health
Interest Area
Academic Health Centers-Investigative Sites
Advertising & Promotion
Biotechnology
Clinical Data Management
Clinical Data Management - eClinical
Clinical Research
Clinical Safety & Pharmacovigilance
Clinical Supplies
CMC
CMC-GMP
Combination Products
Comparative Effectiveness
Document & Records Management
eClinical
Finance
Good Clinical Practices & QA
Information Technology
Manufacturing
Marketing & Sales
Medical Communications
Medical Devices & Diagnostics
Medical Science Liaison
Medical Writing
Non-clinical Safety
Outsourcing
Patient Engagement
Pharmaceutics
Pricing - Reimbursement
Professional Education - Training & Development
Project Management
Public Policy - Health Care Compliance - Law
Public Policy - Law
QA-QC
Quality Assurance - Quality Control
R&D - Strategic Issues
Rare - Orphan Diseases
Regulatory Affairs
Statistics
Strategic Planning
Study Endpoints
Submissions
Val - Electronic Info Integrity
Popular