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Type: 01: ClinSafety-PV, Session [clear filter]
Monday, June 26
 

10:45am EDT

#101: Artificial Intelligence: Delivering on the Promise Room 205 BC #112: Applying Implementation Science Methods to Generate Evidence to Improve Access to New Therapeutics: What has Been Learned? Room 104 AB

1:30pm EDT

#125: Enhancing the Quality of Safety Data Collection Room 205 BC

4:15pm EDT

#156: What's Next in Precision Medicine? Translational Strategies for Dose Optimization in the Age of Project Optimus Room 102
 
Tuesday, June 27
 

8:30am EDT

#212: Full Exposure: Artificial Intelligence to Advance, Replace, and Add Efficiency for Patient Benefit Room 210 #201: Completing the Risk Management Cycle: Review of Risk Management Effectiveness Room 205 BC

10:30am EDT

#216: Benefit-Risk Balance for Medicinal Products: CIOMS Working Group XII Report Room 205 BC

1:15pm EDT

#242: Novel Methods for Signal Identification for Medicines and Medical Devices Room 205 BC #249: Pharmacovigilance: Regulator's Perspectives on Quality Approaches to Additional Risk-Minimization Measures and Post-Pandemic Inspection Reflections Room 253 B

2:30pm EDT

#258: Roundtable Discussion: Benefit-Risk Balance for Medicinal Products: CIOMS Working Group XII Report Grand Ballroom Zone 2

4:00pm EDT

#268: Smarter Approaches to Pharmacovigilance Challenges Room 205 BC
 
Wednesday, June 28
 

8:30am EDT

#301: Using Real-World Data to Evaluate Safety Signals Room 205 A #302: Pharmacovigilance in Africa: Nigeria and Ghana Health Authorities Share their Perspectives Room 205 BC

10:30am EDT

#315: Opportunities to Improve Risk Minimization Outcomes with Behavioral Science Room 253 C

1:15pm EDT

#339: Operationalizing FDA Medical Queries Room 205 BC

2:30pm EDT

#353: Roundtable Discussion: Operationalizing FDA Medical Queries Grand Ballroom Zone 1

4:00pm EDT

#362: Assessing Safety in Rare Disease and Gene Therapy Room 205 BC #373: From 1000's of Tables to Summarizing and Interactively Exploring Clinical Trials Data Room 102
 
Thursday, June 29
 

8:30am EDT

#401: Implementing the Program Safety Analysis Plan and Enhancing Ongoing Aggregate Review with an Interactive Open-Sourced Tool Room 205 BC #405: CIOMS: What it Does and the Guideline on Patient Involvement in the Development, Regulation, and Safe Use of Medicines Room 205 A
 
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Monday, June 12
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Monday, June 26
Tuesday, June 27
Wednesday, June 28
Thursday, June 29
Ballroom Lobby 3
Content Hub NE Lobby
DIA Booth #539 EH
Exhibit Hall
Exhibit Hall Entrance
Exhibit Hall South
Exhibit Hall Theater #1
Exhibit Hall Theater #2
Exhibit Hall Theater #3
Grand Ballroom
Grand Ballroom Zone 1
Grand Ballroom Zone 2
Grand Ballroom Zone 3
Grand Ballroom Zone 3A
Grand Ballroom Zone 3B
North Lobby
Outside Room 210
Room 102
Room 104 AB
Room 151
Room 153 AB
Room 156
Room 157 AB
Room 157C
Room 204
Room 205 A
Room 205 BC
Room 206
Room 210
Room 252
Room 253 A
Room 253 B
Room 253 C
Room 254
Virtual
  • 00: Plenary
  • 01: ClinSafety-PV
  • 02: ClinTrials -ClinOps
  • 03: Data-Tech
  • 04: MedAffairs-SciComm
  • 05: Patient Engagement
  • 06: TranslationalScience-PrecisionMedicine
  • 07: ProjectManagement-StrategicPlanning
  • 08: RD Quality-Compliance
  • 09: Regulatory
  • 10: RegCMC-Product Quality
  • 11: Statistics
  • 12: Value-Access
  • 13: ProfDevelopment
  • 14: DIAmond
  • 15: Content Hubs
  • 16: Community Rounds
  • 17: Networking Opportunities
  • 18: Posters
  • 19: InnovationTheaters
  • 20: Short Courses
  • Level
  • Advanced
  • Basic
  • Intermediate
  • Featured Topics
  • Artificial Intelligence (AI)
  • Benefit - Risk
  • Cell and Gene Therapy
  • Decentralized Clinical Trials (DCTs)
  • Digital Technology
  • Diversity Equity and Inclusion (DEI)
  • Dose Optimization
  • Endpoints
  • Ethics
  • Patient Focused
  • Rare Disease
  • Real-World Data (RWD) - Real-World Evidence (RWE)
  • Regulator Thinking
  • Regulatory Collaboration
  • Student Programming