The Future of Clinical Document Submissions – 3 Strategies to Protect Your Brand 

March 4, 2021 | 2:00PM-3:00PM  EST

This Solution Provider Webinar is brought to you by DIA in cooperation with Privacy Analytics


In This Webinar...

In this session, we’ll discuss the three strategies you need to consider when planning your approach to submitting clinical trial assets in 2021. As privacy concerns continue to make headlines in the pharmaceutical space, sponsors face growing pressure to meet ever stricter regulatory requirements to anonymize clinical trial document submissions. To stay resilient, your organization must employ an approach that shields it from further regulatory shifts.

Learning Objectives:    
  • Recognize what statistical anonymization is and how it can be applied to clinical documents
  • Evaluate whether to do anonymization in-house, with software, or through a service provider
  • Identify the strategic benefits of joining an engaged community of thought leaders 

Featured Topics:
  • Globally accepted best practices for document anonymization 
  • How to produce insight-rich clinical documents that are safe for public sharing
  • The role of knowledge exchange in protecting against unforeseen regulatory demands  


  Niamh McGuinness, BPharm, PHD, Senior Analyst,   Clinical Trial Transparency, Privacy Analytics   
Kniola Lukasz (002).jpg   Lukasz Kniola, Principal Analyst - Data Sharing,   Biogen
Brown, Sabrina.jpg
  Sabrina Brown, Expert Transparency Manager,     Novartis Pharmaceuticals Corporation