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DIA 2024 Global Annual Meeting
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DIA 2024 Global Annual Meeting
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00: Plenary
All
Forum
01: ClinSafety-PV
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Forum
Session
Workshop
02: ClinTrials -ClinOps
All
Forum
Session
Workshop
03: Data-Tech
All
Forum
Session
Workshop
04: MedAffairs-SciComm
All
Forum
Session
Workshop
05: Patient-Focused Drug Dev
All
Forum
Session
Workshop
06: TranslationalDelivery Tech-PrecMedicine
All
Forum
Session
07: ProjectManagement-StrategicPlanning
All
Forum
Session
08: RD Quality-Compliance
All
Forum
Session
Tutorial
09: Regulatory
All
Forum
Session
Workshop
10: RegCMC-Product Quality
All
Forum
Session
Workshop
11: Statistics-Data Science
All
Forum
Session
Workshop
12: Value-Access
All
Forum
Session
Workshop
13: ProfDevelopment
All
Forum
Session
Tutorial
Workshop
14: DIAmond
All
Forum
15: Content Hubs
All
Workshop
16: Community Rounds
All
Session
17: Networking Opportunities
All
Session
Social Event
Social Evt / Reception
18: Posters
All
Session
19: InnovationTheaters
All
Session
20: Networking Opportunities
All
Session
20: Short Courses
All
Tutorial
Blood Drive
All
Social Event
Format
Forum
Session
Tutorial
Workshop
Level
Advanced
Basic
Intermediate
Featured Topics
Artificial Intelligence (AI)
Cell and Gene Therapy
Decentralized Clinical Trials (DCTs)
Digital Technology
Diversity Equity and Inclusion (DEI)
Ethics
ICH
Patient Focused
Rare Disease
Real-World Data (RWD)- Real-World Evidence (RWE)
Regulator Perspectives
Regulatory Collaboration
Regulatory Reliance
Risk Management
Special Populations
Student Programming
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Schedule
Speakers
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Steve Winitsky
Parexel International, United States
Vice President, Technical
RW
Rodney Winley
CSL Behring, United States
Head, R&D Patient Partnerships
Kathleen Winson
Genentech, A Member of the Roche Group, United States
Executive Group Director, Product Development Regulatory
AW
Amy Wise
AbbVie, United States
Associate Director, RA Device and Combination Products
Steven Woloshin
Dartmouth Institute, United States
Professor
Olivia Wong
Gilead, United States
Director, Quality, Combination Products
Karen Wood
Medidata , United States
Senior Manager Patient Advocacy
George Wu
Gilead, United States
Director, Biostatistics
YW
Yangfeng Wu
Peking University Clinical Research Institute, China
Executive Director
Satomi Yagi
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Reviewer, Office of New Drug III
Xiaojun (Wendy) Yan
BeiGene (Beijing) Co., Ltd., China
Senior Vice President, Chief Regulatory Officer
FY
Felix Yang
Genentech, A Member of the Roche Group, United States
US Regulatory Policy Fellow
Ling Yang
FDA, United States
Senior Physician, OSI, OC, CDER
Scarlett Yang
Gilead Sciences, United States
Senior Regulatory Affairs Associate
Zhimin Yang
National Medical Products Administration (NMPA), China
Deputy Director, Center for Drug Evaluation
Lynne Yao
FDA, United States
Director, Division of Pediatric and Maternal Health, Office of New...
Debra Yeskey
CEPI, United States
Head of Regulatory Policy and Intelligence
Clarence Young
Propharma, United States
Senior Vice-President, Clinical, US Regulatory Sciences
Jiangyong Yu
National Medical Products Administration (NMPA), China
Director, Department of Drug Registration
Lawrence Yu
FDA, United States
Director, Office of New Drug Products, OPQ, CDER
Shou Yuan
Taimei Technology Inc., United States
Product Innovation and Global Operations Representative
Sunita Zalani
Merck & Co., Inc., United States
Vice President, Regulatory Affairs, Oncology
MV
Mui Van Zandt
IQVIA, United States
VP/Global Head, Data Strategy, Access and Enablement
JZ
Jiewei Zeng
Abbvie, United States
Associate Director
Yueqin Zhao
FDA, United States
Lead Mathematical Statistician, OB, OTS, CDER
Hao Zhu
FDA, United States
Division Director, Division of Pharmacometrics, OCP, OTS, CDER
Yao-Yao Zhu
AstraZeneca, United States
Regulatory Affairs Director
Bianca Zimon
ANVISA, Brazil
Health Regulation Specialist
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