Pragmatic Statistical De-Identification

Brian Rasquinha, Associate Director, Solution Architecture at Privacy Analytics, will be moderating a panel discussion on Pragmatic Statistical De-Identification. Guest panelists: Lauren Groebe, ...

Informa Connect Clinical Data Disclosure, Transparency and Plain Language Summaries U.S. Conference

Obaraboye Olude, Privacy Analytics’ Senior Clinical Trial Transparency Advisor and Manager will be presenting this Case Study with Craig Tipple, Medical Director at DNDi on Tuesday, February 25 ...

Transparency-by-Design: Build Efficiencies into Your Clinical Document Disclosure Process

Abby McDonell, Privacy Analytics’ Senior Program and Project Manager, Clinical Trial Transparency, will be presenting at the Conference on Thursday, November 7 (10:00am–10:30am CET)

Privacy Regulation and Real-World Applications for Generative AI in Healthcare

Santa Borel, Associate Director, Data Privacy Solutions at Privacy Analytics will be moderating a panel discussion on Privacy Regulation and Real-World Applications for Generative AI in Healthcare. ...

IAPP’s Privacy. Security. Risk. Conference

Privacy Analytics will be exhibiting (booth #419) at IAPP’s Privacy. Security. Risk. Conference September 23-24, 2024 in Los Angeles.

Privacy + Security Academy’s Spring Forum

Brian Rasquinha, Associate Director, Solution Architecture at Privacy Analytics will be moderating a panel discussion on Using De-Identification to Safely Enable Innovation and Commercialization. ...

Transparency-by-Design: Build Efficiencies into Your Clinical Document Disclosure Process

8:00 AM or 11:00 AM Eastern Standard Time Duration: 30 minutes

Informa Connect Clinical Data Disclosure Europe Conference

Niamh McGuinness, Senior Advisor, Clinical Trial Transparency and Privacy, will be presenting at the Conference on November 6 (3:00pm - 3:35pm CET).

IAPP’s Privacy. Security. Risk. Conference

Privacy Analytics will be exhibiting (booth #615) at IAPP’s Privacy. Security. Risk. Conference October 5-6 in San Diego.

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.

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 ...

3 Ways to Safely Accelerate Your Clinical Document Submissions

As a clinical trial sponsor, you were already facing tight timelines and resource constraints in handling regulatory requirements for document anonymization and redaction.

Innovate Throughout the Data Life Cycle

Time: 1 p.m. ET (3 hour workshop + 1 hour networking)

Safely Innovating with Sensitive Data

If you’re looking to safely use and share your organization’s sensitive data while earning trust from stakeholders, this LinkedIn Live Event is for you.

DIA’s Real World Evidence Conference

This conference will explore new and innovative applications of RWE, and deliver cutting-edge insights in how stakeholders are leveraging RWE to advance healthcare knowledge and decision-making.

3rd Real World Evidence and Data Insights Conference

This conference will help you better understand and develop strategies for streamlining RWE & RWD collection and usage in order to ensure patient safety, satisfy regulatory compliance, and ...

9th Annual Publication and Clinical Trial Transparency Conference

Beyond Data Transparency: Innovation Across the Drug Development Lifecycle

Informa Connect Clinical Data Disclosure, Transparency and Plain Language Summaries U.S. Conference

Niamh McGuinness, Associate Director, Safety, Regulatory & Transparency Senior Advisor, will be presenting at the Conference on March 19 (10:25am– 11:00am ET).

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