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Type: 04: MedAffairs-SciComm, Session [clear filter]
Monday, June 20
 

4:00pm CDT

#133: New Tools for Creating Flexible and Sustainable Master Protocols Room 176
 
Tuesday, June 21
 

9:00am CDT

#206: The Future of Content Authoring and Web Portal Technology, Publishing Stability Calculators: Challenges for Pushing Automation Room 470 B

9:15am CDT

#209: New EU Clinical Trial Regulation: Experience So Far Room 184

11:00am CDT

#221: Complying with the EU-CTR Disclosure Standards in the Era of GDPR Room 470 B

11:15am CDT

#227: Approaching the Assessment of Clinical Protocol Complexity Room 183 C

1:45pm CDT

#245: Understanding the Consumer's Journey for Information From Searching for Information to Using Information Room 180
 
Wednesday, June 22
 

11:15am CDT

#324: The Value of Medical Writing: The Regulator's Perspective, Development of Professional Medical Writers as Successful Leaders Room 183 C

12:30pm CDT

#334 RT: Round Table Discussion: The Value of Medical Writing: The Regulator's Perspective, Development of Professional Medical Writers as Successful Leaders Room 375 A Zone 1
 
Thursday, June 23
 

10:00am CDT

#408: Writing at Lightspeed: Optimizing Submission Dossiers in Today’s Environment Through Better Processes, Planning, and Technology Room 180
 
Monday, June 26
 

1:30pm CDT

Consent is the Oil of Customer Engagement: How to Keep the Omnichannel Engine Running TBD

4:15pm CDT

Best Practices in Effective Gathering of Medical Information Industry Insights TBD
 
Tuesday, June 27
 

8:30am CDT

Innovation Across Medical Affairs Throughout the Global Pandemic TBD

10:30am CDT

Medical Storytelling Inserted Into All Aspects of Medical Affairs TBD

1:15pm CDT

Tech-Enabled Narratives: Technology Meets Process FTW (For the Win!) TBD
 
Wednesday, June 28
 

8:30am CDT

Writing Summary Documents for Rare Disease Submissions: Unique Challenges TBD

10:30am CDT

Is the Hype Real? Real-Life User Experience of Medical Writing Artifcial Intelligence Tools for Clinical Study Reports Production TBD

1:15pm CDT

Estimands and Designing of the Clinical Trial and Protocol Structure TBD
 
Thursday, June 29
 

8:30am CDT

A Global Sponsor Perspective on Implementation of the New EU Clinical Trials Regulation TBD
 
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Exh Hall Community Area
Exhibit Hall
Exhibit Hall Booth #1719
Exhibit Hall Theater #1
Exhibit Hall Theater #2
Exhibit Hall Theater #3
Level 3 F2 Entrance
Meeting Rm Lobby Level 1
Meeting Room Lobby
Room 175
Room 176
Room 178
Room 179
Room 180
Room 183 A
Room 183 B
Room 183 C
Room 184
Room 185 AB
Room 185 CD
Room 186
Room 187
Room 375 A Zone 1
Room 375 A Zone 2
Room 470 A
Room 470 B
Room 471 A
Room Skyline 375 CDE
Skyline Ballroom Foyer
TBD
Virtual
  • 00: Plenary
  • 01 - Clinical Safety and Pharmacovigilance
  • 01: ClinSafety-PV
  • 02: ClinTrials -ClinOps
  • 03: Data-Tech in Clinical Trials
  • 04: MedAffairs-SciComm
  • 05: Patient Engagement
  • 06: PreClinical Dev-EarlyPhaseCR
  • 06 - Translational Sciences and Precision Medicine
  • 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
  • AI and Machine Learning
  • COVID-19
  • Data Science
  • Decentralized Trials
  • Digital
  • Diversity Equity and Inclusion
  • Innovative Trial Design
  • Patient Perspective
  • Personalized Health Care
  • Regulator Perspective
  • Remote Work
  • RWD-RWE
  • Special Populations
  • Student Programming