Webinars

Webinars | Date of Event: October 14, 2025
De-identified ≠ risk-free: What health systems need to know about data linkage

Linking de-identified datasets can unlock critical value for research and AI — but without the right safeguards, it also raises serious privacy risks.
Webinars | Date of Event: May 22, 2025
How to de-identify (almost) anything

Join this webinar to explore how leading organizations are expanding their understanding and approaches to broadening data types to enable innovation.
Webinars | Date of Event: November 7, 2024
Transparency-by-Design: Build Efficiencies into Your Clinical Document Disclosure Process

Join Abby McDonell, Sr. Program Manager with IQVIA’s Clinical Trial Transparency Team (powered by Privacy Analytics), to gain actionable insights on optimising your medical writing processes to ...
Webinars | Date of Event: September 12, 2024
10 Best Practices for ROI on HIPAA Expert Determination

In this webinar, we’ll explore 10 non-technical best practices for HIPAA Expert Determination aimed at reducing timelines, rework, and costs while maximizing the organizational benefit from the data ...
Webinars | Date of Event: May 23, 2024
Linkage, Tokenization and De-identification

Watch this replay of our webinar to learn about tokenization and how it can be used to match individuals without exposing key identifiers, the risk of re-identification and how it can increase when ...
Webinars | Date of Event: March 19, 2024
CASE STUDY Navigating a First-Time Health Canada PRCI Submission: Learnings and Perspectives from Argenx and Privacy Analytics

Watch this replay of our presentation at Informa Connect’s Clinical Data Disclosure, Transparency and Plain Language Summaries U.S. Conference and hear some perspectives on collaborative best ...
Webinars | Date of Event: November 6, 2023
Using Technology to Streamline the Publication of Anonymized Clinical Trial Documents and Protect CCI

Watch this replay of our presentation at Informa's Clinical Data Disclosure Europe event to hear about solutions to some of the common challenges in clinical trial document and data disclosure.
Webinars | Date of Event: June 1, 2023
Everything You Need to Know About EMA Policy 0070 Right Now

On May 16, the European Medicines Agency (EMA) confirmed that after a long hiatus (punctuated only by COVID-related publications), Policy 0070 will officially resume in September 2023. Join Niamh ...
Webinars | Date of Event: March 9, 2023
Safely Accelerate Clinical Document Submissions While Protecting Commercially Confidential Information (CCI)

As a clinical trial sponsor, you’re under tight timelines to balance participant privacy and data utility in clinical document submissions while justifying and protecting commercially sensitive ...
Webinars | Date of Event: January 19, 2023
How to Protect Your Company’s Commercial Interest Under EU CTR

As a clinical trial sponsor, you’re under pressure to be transparent, but how do you ensure your clinical study documents don’t reveal confidential trade secrets when published by regulators?

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