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3rd Disclosure and Transparency For Clinical Data Summit

August 14 @ 8:00 am - August 15 @ 3:45 pm

 

 

3rd Disclosure and Transparency For Clinical Data Summit

 

To register, please click here

 

The 3rd Disclosure and Transparency for Clinical Data Summit will convene on August 14-15 in PhiladelphiaView the agenda.

Join industry experts as we define standardization processes for disclosure and registry, provide best practices to balance commercial confidentiality and public access, and examine proven tactics that preserve data usage while ensuring anonymization. This Summit will provide the tools needed to maximize the benefits of clinical data from the inherent risks of clinical trials, all while complying with national and global compliance regulations.

 

 

The life science and clinical data transparency industry must take a collaborative approach to achieve data disclosure compliance to combat the burden of new regulatory requirements and renewed infrastructure needs. Within these new regulatory changes, both the U.S and global level develop strategies to release patient-level data and anonymous data to achieve meaningful patient engagement.

At ExL’s 3rd Disclosure and Transparency for Clinical Data Summit, attendees will gain comprehensive, high-quality education that balances commercial values and ethical responsibility through the execution of national and global data transparency.

 

Top Five Reasons to Attend

  1. Understand the impact of GDPR on sharing and clinical trial data
  2. Gain insight on utilizing clinical data and view data sharing
  3. Discuss best practices for managing global disclosure
  4. Differentiate legal perspectives and legal procedures for data sharing
  5. Improve communications to achieve patient involvement

 

Who Should Attend

This conference is designed for professionals from pharmaceutical companies with responsibilities in the following areas:

  • Clinical Trial Disclosure and Transparency
  • Clinical Trial Information Disclosure/Management
  • Clinical Operations
  • Data Management/Standards
  • Regulatory Affairs
  • Clinical Trial Registration
  • Publication Planning
  • Medical Writing
  • Information/Knowledge Management
  • Strategic Projects Management
  • Medical Communications
  • Patient Engagement
  • Biostatistics/Bioinformatics

This event is also of interest to:

  • Data Reporting/Transparency Solution Providers
  • Medical Writing/Publication Services
  • Discrepancy Management/Data Management Service Providers
  • Legal Consultants

 

 

 

Featured Sessions

The Future of Healthcare: Understanding the Use of AI and Blockchain in Patient-Level Data Sharing

 
Bob Stewart
 
 

Bob Stewart, Board Member and Chief Technology Officer, THE ALLIANCE FOR CLINICAL RESEARCH EXCELLENCE AND SAFETY (ACRES)

 

Discuss Responsible Clinical Data Sharing for Better Patient Outcomes

 
Asba Tasneem
 
 

Asba Tasneem, Informatics Portfolio Leader, Data Sharing Lead , DCRI, DUKE CLINICAL RESEARCH INSTITUTE

 

Using Quality by Design to Simplify Clinical Trial Start-up and Disclosure Compliance

 
Joyce Hauze

Joyce Hauze, CCRA, ACRP-PM, Associate Director, Clinical Trial Disclosure and Transparency, MALLINCKRODT PHARMACEUTICALS

 
 
Mary Brantner

Mary Brantner, Senior Director, Head of Global Development Operations Process and Systems, MALLINCKRODT PHARMACEUTICALS

 

What Disclosure and Transparency Look Like From the Patients’ View

 
Deborah Collyar
 
 

Deborah Collyar, President, PATIENT ADVOCATES IN RESEARCH (PAIR)

 

Details

Start:
August 14 @ 8:00 am
End:
August 15 @ 3:45 pm
Website:
https://exlevents.com/disclosureandtransparency

Organizer

ExL Events
Phone:
For information on speaking opportunities, please contact Warren Drysdale at wdrysdale@exlevents.com or 917-258-5162.
Email:
For information on sponsorship or exhibition opportunities, please contact Jayson Mercado at jmercado@exlevents.com or 212-400-6236.
Website:
http://exlevents.com