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DIA 2016 Annual Meeting
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Preconference Tutorial
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Trk 01: Clinical Operations
All
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Trk 02: Proj-Port Mgt-Strat Planning
All
Forum
Session
Workshop
Trk 02: Proj/Port Mgt/Strat Planning
All
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Trk 03: Innov Part Model-Outsourcing
All
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Trk 03: Innov Part Model/Outsourcing
All
Session
Trk 04: Preclin Transl-Early Clin Dev
All
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Session
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Trk 05: Reg of Prod Adv-Mkting
All
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Session
Trk 05: Reg of Prod Adv/Mkting
All
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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
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Trk 08: Reg Affairs
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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
Tutorial
Trk 10: Pub Pol/HealthCare Compl/Law
All
Forum
Session
Trk 11: Quality in CT-GCP
All
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Tutorial
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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Session
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Trk 13: CER/Glob Health Econ
All
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Session
Trk 14: Clin Safety-PV
All
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Session
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Trk 14: Clin Safety/PV
All
Session
Trk 15: Statistics
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Session
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Trk 16: Prof Development
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Session
Tutorial
Workshop
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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Trk 23: Opening Plenary
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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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Tuesday
, June 28
8:00am EDT
#202: Changing Cultures to Advance Patient Engagement
103ABC
#203: Next Generation Collaborations: Transforming the Industry
Ballroom A
#201: International Regulatory Convergence, Collaboration, and Cooperation
114
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
#215: Exploring the Use of Virtual Technologies and Virtual Teams Within Medical Affairs Organizations
202AB
#218: Lessons Learned from Eight Years of Drug Development Tool/Novel Methodology Qualification
201B
#220: Regulatory Changes in China and the Impact to Global Drug Development Planning
109AB
#222: Valuing the Clinical Trial Patient
204A
#224: Identifying Patient-Centered Outcomes for Use in Observational Research: Why and How
201A
#227: Unique Global Regulatory Considerations and Drug Development Incentives in Rare Disease and Orphan Drug Development
103C
#208: Measuring Return on Engagement: An Interim Report on the DIA-Tufts CSDD Metrics Study
108B
#209: The Promotable Project Manager: Leadership Behaviors Critical to Success in the Life Sciences
102AB
#211: Collaboration with a Purpose
111AB
#212: Special Populations in Clinical Pharmacology Studies
113A
#214: Product Management Strategies: Maximizing Content Re-Use to Meet Diverse Customer Information Needs
203AB
#217: Electronic Submissions Gateway: Next Generation
201C
#216: Implementing a Successful Metadata Repository: The Journey of a Thousand Milestones Begins with a Single Step
204C
#221: Envision the Future: How Big Data and Artificial Intelligence Change Our Regulatory Environment
103A
#223: Global Harmonization: Current ICH Quality Initiatives
112AB
#226: The Global Conundrum: Herding Cats - Identifying Risk Across Pharmacovigilance Networks and Seeking Simplicity in Multi-Country Pharmacovigilance Activities
113C
#225: One Size Does Not Fit All: Best Practices for Right-Sized Signal Management Systems
113B
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
12:40pm EDT
#232: PRA Innovation Theater: Transforming EMR to EDC
Exhibit Hall B
1:20pm EDT
#233: Veeva Innovation Theater: The Great RIM Throwdown! How Are You Managing Regulatory Events?
Exhibit Hall B
2:00pm EDT
#237: Acquisitions and Mergers: When Companies’ Regulatory Operations Systems and Processes Converge
112AB
#253: Update from Health Canada
202AB
#234: TransCelerate's Risk-Based Monitoring: Sharing What We Are Learning
109AB
#236: Expanded Access: Ethical, Regulatory, and Policy Challenges and Considerations
108B
#239: Cloud Compliance: Clinical Software Challenges and Vendor Auditor Views
201C
#241: Disease Interception: Shifting the Paradigm from Treatment to Prevention of Disease
201B
#242: Regulatory Challenges in the Development of Combination Products Involving Digital Technology
108A
#243: Patient Involvement Today and Tomorrow: What’s in It for Patients?
204C
#244: Transforming Clinical Development Through Enterprise Quality Management
204A
#245: Risk-Based Inspections
111AB
#246: Valuing the Signal and the Noise in Health Care Horizon Scanning
103A
#249: Current Topics for Pharmacovigilance in Japan
113B
#250: Open-Label, Long-Term Extension Studies: Study Designs and Ethics
201A
#254: CBER Town Hall: State of the Center and Plans for the Future
203AB
3:25pm EDT
#256: Veeva Innovation Theater: 2016 Paperless TMF Survey: Trends and Insights
Exhibit Hall B
4:00pm EDT
#262: Solving Challenges and Employing Best Practices in Medical Information Contact Centers
201A
#269: Making Quality Stick: Building a Complete Quality Culture
204A
#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
#259: Innovative Regulatory Solutions: Utilizing Flexible Outsourcing Strategies
112AB
#260: A Risk-Benefit Approach to Planning Early Clinical Development
113C
#261: Marketing After Amarin and Pacira
107AB
#263: Patient Centricity in Clinical Trials
201B
#264: FDA Update on Data Standards
204B
#265: Enabling Innovative New Endpoint Measurement Using Mobile Technology
203AB
#266: Perspectives on Expanded Access to Investigational New Drugs
108A
#267: FDA Institutes/Centers of Excellence: A Step Toward Patient Focused Drug Development?
105AB
#268: Emerging Biopharma Therapeutic Modalities: Scientific and Policy Implications
201C
#270: Implementing Knowledge Management: Industry Perspectives
111AB
#271: The Things Kids Say: Clinical Outcome Assessments in Pediatric Clinical Trials
103A
#272: How Can We Build Reliability and Quality When Outsourcing Pharmacovigilance?
113B
#273: Improving Adverse Drug Reaction Information in Product Labels
109AB
#274: Statistical Issues in the Evaluation of Biosimilars
108B
#276: Using Input from Patient Communities to Develop PRO Instruments
103C
#277: PMDA Town Hall
202AB
Timezone
DIA 2016 Annual Meeting
America/New York
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DIA 2016 Annual Meeting
Jun 25
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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 15: Statistics
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Trk 16: Prof Development
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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
All
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Trk 23: Opening Plenary
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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 26
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, June 28
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, June 29
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, June 30
Venue
102AB
103A
103ABC
103C
104A
104AB
105AB
107AB
108A
108B
109AB
111AB
112AB
113A
113B
113C
114
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202AB
203AB
204A
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204C
Ballroom A
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Exhibit Hall
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Liberty Ballroom A
TBA
TBD
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Preconference Tutorial
All
Tutorial
Trk 01: Clinical Operations
All
Forum
Session
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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
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Symposium
Trk 03: Innov Part Model/Outsourcing
All
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Trk 04: Preclin Transl-Early Clin Dev
All
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Trk 05: Reg of Prod Adv-Mkting
All
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Trk 05: Reg of Prod Adv/Mkting
All
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Trk 06: Med Comm-Wrtg-MSL
All
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Trk 06: Med Comm/Wrtg/MSL
All
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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 08: Reg Affairs
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Trk 09: Med Devices-InVitro-CombProd
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Trk 09: Med Devices/InVitro/CombProd
All
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Trk 10: Pub Pol-HealthCare Compl-Law
All
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Trk 10: Pub Pol/HealthCare Compl/Law
All
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Trk 11: Quality in CT-GCP
All
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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
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Trk 16: Prof Development
All
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Workshop
Trk 17: Rare-Orphan Diseases
All
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Trk 17: Rare/Orphan Diseases
All
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Trk 18: Global Regulatory
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Trk 19: DIAmond
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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
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