| PHUSE US |
2026 |
Anonymisation Strategies for Policy 0070 and PRCI Submissions [presentation] |
Stuart Donald |
source |
16 |
| PHUSE US |
2026 |
Anonymization Insights from 2025 [presentation] |
Honz Slipka |
source |
11 |
| PHUSE US |
2026 |
From Complexity to Consistency: Scalable Anonymization Across Clinical Trial Portfolios [presentation] |
Ahmed Eldafrawy, Danielle DiBonaventura |
source |
22 |
| PHUSE EU |
2021 |
Navigating the Evolving Regulations for Health Canada [presentation] |
Gina Bennet |
source video |
20 |
| PHUSE US |
2021 |
A Quantitative and Metrics-driven Framework for Maximizing Data Utility While Balancing Re-identification Risk [presentation] |
Stephen Doogan |
source video |
18 |
| PHUSE US |
2021 |
Software Demonstration: SD11: Streamline Your Quantitative Anonymization Process and Deliver Consistent Outputs for Every Disclosure Scenario [presentation] |
Stephen Doogan |
source |
8 |
| PHUSE EU |
2020 |
Achieving Balance - Approaching Anonymisation with Quantified Risk [presentation] |
Cathal Gallagher |
source video |
27 |
| PHUSE US |
2020 |
A Case Study: Data Transparency of Clinical Trial Data |
Sherry Meeh |
source presentation source |
8 |
| PHUSE EU |
2019 |
Integrated Data and Document Anonymisation for Efficient Data Sharing [presentation] |
Ali Dootson, Cathal Gallagher |
source |
27 |
| PHUSE EU |
2017 |
Assessing New CFDA Requirements on Data Integrity Using Risk-Based Monitoring and Enrollment Patterns |
Wenjun Bao, Richard C. Zink, Geoffrey A. Mann |
source presentation source |
13 |
| PHUSE EU |
2016 |
A Standardised Approach to De-identification |
Christopher C. Hurley |
source presentation source |
13 |
| PharmaSUG |
2014 |
Risk-Based Monitoring of Clinical Trials Using JMP Clinical |
Richard C. Zink, Kelci J. Miclaus |
source |
15 |
| SGF |
2014 |
Risk-Based Monitoring of Clinical Trials Using JMP Clinical |
Richard C. Zink |
source |
14 |