Webinars

Join this webinar to explore how leading organizations are expanding their understanding and approaches to broadening data types to enable innovation.

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 simplify downstream disclosure and transparency initiatives while ensuring participant and commercial data privacy remains protected.

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 de-identification project.

In this webinar, Brian Rasquinha, Associate Director of Solution Architecture at Privacy Analytics dives into tokenization and data de-identification to further your understanding of privacy-preserving data practices.

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.

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 McGuinness, Senior Advisor, Clinical Trial Transparency and Privacy, to learn the key points of EMA's announcement.

Join Niamh McGuinness, Senior Advisor, Clinical Trial Transparency and Privacy, to find out how Privacy Analytics offers a complete, end-to-end solution for your clinical document submissions.

Join Niamh McGuinness, Senior Advisor, Clinical Trial Transparency and Privacy, to find out how Privacy Analytics can help you to meet your regulatory submission deadlines while protecting patient privacy and identifying and protecting commercially confidential information (CCI).

Watch the replay with Niamh McGuinness, Senior Manager of Clinical Trial Transparency and Privacy, Privacy Analytics, to learn about three solution options to help you meet your regulatory submission deadlines while protecting patient privacy and CCI.

In this panel replay, you’ll get tangible strategies and tactics to identify, substantiate and communicate a compelling, urgent reason to provide internal access to sensitive data or to share sensitive data assets externally.