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DIA 2016 Annual Meeting
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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 05: Reg of Prod Adv/Mkting
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Trk 06: Med Comm-Wrtg-MSL
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Trk 06: Med Comm/Wrtg/MSL
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Trk 07: Tech-Data- Records-Subs
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Trk 07: Tech/Data/ Records/Subs
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Session
Symposium
Trk 08: Reg Affairs
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Session
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Trk 09: Med Devices-InVitro-CombProd
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Trk 09: Med Devices/InVitro/CombProd
All
Session
Trk 10: Pub Pol-HealthCare Compl-Law
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Session
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Trk 10: Pub Pol/HealthCare Compl/Law
All
Forum
Session
Trk 11: Quality in CT-GCP
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Tutorial
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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Session
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Trk 13: CER/Glob Health Econ
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Session
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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Workshop
Trk 17: Rare-Orphan Diseases
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Trk 20: Innov Theater
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RN
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Advanced
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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
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Vaccines
Value-Based Evidence
Women's Health
Interest Area
Academic Health Centers-Investigative Sites
Advertising & Promotion
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CMC
CMC-GMP
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Comparative Effectiveness
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Marketing & Sales
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Medical Devices & Diagnostics
Medical Science Liaison
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Pharmaceutics
Pricing - Reimbursement
Professional Education - Training & Development
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Public Policy - Health Care Compliance - Law
Public Policy - Law
QA-QC
Quality Assurance - Quality Control
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Regulatory Affairs
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Study Endpoints
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Val - Electronic Info Integrity
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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
#117: IDMP: A Compliance Project or a New Way of Conducting Business?
109AB
#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
#104: Impact of Biologics, Vaccines, Oncology, and Breakthrough Therapy Designation on Traditional Global Drug Development Strategy
105AB
#105: Maximize the Value of Your Product by Beginning with the End in Mind
107AB
#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
#108: Drug/In Vitro Diagnostic Device Advertising and Promotion: Unapproved Combination Product or Awareness?
203AB
#109: EHR in Clinical Research: Heralding a New Era
201C
#110: Updates and Pending Issues in the US Biosimilar Environment
201B
#111: Global Regulatory Harmonization in Asia: Is a New Trend Occurring?
204B
#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
#115: Clinically Relevant Specifications: Translating Voice of the Patient Into Quality Attributes of the Product
111AB
#116: Has the EU Good Pharmacovigilance Practices Delivered on Its Intended Promise and Commitment?
103C
#118: The Interpretation of PRO Scores and Responder Analyses in the Presence of Missing Data
201A
#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
10:45am 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
#127: Innovative Partnerships: gOVERN - A Research and Early Development’s Outsourcing Vision to Enable Resourcing INovation
112AB
#128: Alliance Management Forum
111AB
#129: Delivering Value Through Medical Information Metrics
203AB
#130: Take Two Aspirin and Text Me in the Morning: Technology Suited for 20,000 Virtual Patients on the PCORI Aspirin Trial
201C
#132: Electronic Implementation of New PRO Measures to Assess Treatment Benefit in Irritable Bowel Syndrome Trials: Lessons Learned
204C
#131: IDMP Update
204B
#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
#134: How Can We Utilize Mobile Health for Better Quality of Life and Medical Economy?
103A
#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
#138: Risk Communication and Management: The Art of Communicating Risk - Challenges and Best Practices
109AB
#139: Measuring the Impact and Influence of Patient Input on Regulatory and Health Technology Assessment Decision Making: What Are the Key Considerations?
105AB
#140: Understanding, Developing, and Implementing an Anticipated Events Review Process: Adoption of the FDA IND Rule on Safety Reporting Requirements
108A
#141: Transforming Health Care Data for Clinical Research: Strategy and Experiences from the PCORnet Common Data Model
201A
#143: Priority Review Vouchers: Past Experiences, Legislative Reform, and Tips for Sponsors
103C
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DIA 2016 Annual Meeting
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DIA 2016 Annual Meeting
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102AB
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114
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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
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Trk 02: Proj/Port Mgt/Strat Planning
All
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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 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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Session
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
All
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Trk 20: Innov Theater
All
Session
Trk 21: Poster Presentations
All
Poster Presentation
Trk 22: Engage and Exchange
All
Workshop
Trk 23: Opening Plenary
All
Session
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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Saturday
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, June 30
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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
Tutorial
Trk 01: Clinical Operations
All
Forum
Session
Symposium
Tutorial
Workshop
Trk 02: Proj-Port Mgt-Strat Planning
All
Forum
Session
Workshop
Trk 02: Proj/Port Mgt/Strat Planning
All
Forum
Trk 03: Innov Part Model-Outsourcing
All
Forum
Session
Symposium
Trk 03: Innov Part Model/Outsourcing
All
Session
Trk 04: Preclin Transl-Early Clin Dev
All
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Session
Symposium
Trk 05: Reg of Prod Adv-Mkting
All
Forum
Session
Trk 05: Reg of Prod Adv/Mkting
All
Forum
Session
Trk 06: Med Comm-Wrtg-MSL
All
Session
Symposium
Trk 06: Med Comm/Wrtg/MSL
All
Session
Trk 07: Tech-Data- Records-Subs
All
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Trk 07: Tech/Data/ Records/Subs
All
Forum
Session
Symposium
Trk 08: Reg Affairs
All
Forum
Session
Tutorial
Trk 09: Med Devices-InVitro-CombProd
All
Forum
Session
Trk 09: Med Devices/InVitro/CombProd
All
Session
Trk 10: Pub Pol-HealthCare Compl-Law
All
Forum
Session
Tutorial
Trk 10: Pub Pol/HealthCare Compl/Law
All
Forum
Session
Trk 11: Quality in CT-GCP
All
Forum
Session
Tutorial
Trk 11: Quality in CT/GCP
All
Session
Trk 12: Pharm Quality
All
Forum
Session
Trk 13: CER-Glob Health Econ
All
Forum
Session
Tutorial
Trk 13: CER/Glob Health Econ
All
Forum
Session
Trk 14: Clin Safety-PV
All
Forum
Session
Tutorial
Trk 14: Clin Safety/PV
All
Session
Trk 15: Statistics
All
Forum
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Tutorial
Trk 16: Prof Development
All
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Session
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Workshop
Trk 17: Rare-Orphan Diseases
All
Forum
Session
Symposium
Tutorial
Trk 17: Rare/Orphan Diseases
All
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Trk 18: Global Regulatory
All
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Trk 19: DIAmond
All
Forum
Trk 20: Innov Theater
All
Session
Trk 21: Poster Presentations
All
Poster Presentation
Trk 22: Engage and Exchange
All
Workshop
Trk 23: Opening Plenary
All
Session
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