| PharmaSUG |
2026 |
Accelerating CDISC SEND Conversion with AI: From Raw Preclinical Data to Regulatory-Ready Datasets |
Nattawit Pewngam,
Chotika Chatgasem,
Titipat Achakulvisut |
source |
10 |
| PHUSE US |
2026 |
Advancing Precision Medicine and Regulatory Readiness: Data Harmonisation and Statistical Methods for Companion Diagnostics Bridging Studies |
Ummul Vara Qurratul Ain |
source
presentation source |
10 |
| PHUSE APAC |
2026 |
End-to-End Continuous Integration and Deployment Pipeline for Multi Language Analytics Applications: A Clinical Data Management Case Study |
Avinash Patnaik,
Varun Sethuraman |
source
presentation source |
7 |
| PHUSE APAC |
2026 |
Enhancing Clinical Data Standardization Through Intelligent Mapping of eCRF Forms and Items to SDTM |
Saransh Khandelwal,
Kedar Deshpande |
source
presentation source |
9 |
| PHUSE EU |
2025 |
Framework for Integrating Omics Data with Other Clinical and NonClinical Data Sources |
Mehdi Harek,
Jonathon Keeney |
source
presentation source |
12 |
| PHUSE EU |
2025 |
Turbocharge Your Trials: Transform CRF Creation and the CDISC standardization process with Xbiom's Smart Metadata Repository and AI/ML Integrations |
Harinarayanan Gopichandran |
source
presentation source |
8 |
| PharmaSUG |
2025 |
Elevating Clinical Research: Strategic Implementation of CDASH and SDTM Standards |
Hayden Patel |
source |
4 |
| PharmaSUG |
2025 |
SDTM Transformation through Artificial Intelligence (AI) and Human in the Loop (HITL): Lessons Learnt from Abbvie Case Study |
Aman Thukral,
Sanjay Bhardwaj |
source |
2 |
| PHUSE US |
2025 |
Turbocharge Your Trials: Transform CRF Creation and the CDISC standardization process with Xbiom's Smart Metadata Repository and AI/ML Integrations |
Harinarayanan Gopichandran |
source
presentation source |
8 |
| PHUSE EU |
2023 |
Statistical Programming 101 for the Fourth Industrial Revolution |
Ritika Aggarwal |
source
presentation source |
10 |
| PHUSE US |
2023 |
Helping You Get in the Lightning Lane for a Wild Submissions Ride! [presentation] |
Ali Dootson |
source
video |
20 |
| PHUSE EU |
2022 |
Submission Readiness [presentation] |
Ali Dootson |
source |
16 |
| PHUSE US |
2022 |
Clinical Data Standardization and Integration Using Data Warehouse and Data Mart Processes [presentation] |
Clio Wu |
source |
15 |
| PharmaSUG |
2020 |
Moving A Hybrid Organization Towards CDISC Standardization |
Kobie O'Brian,
Sara Shoemaker,
Robert Kleemann,
Kate Ostbye |
source |
8 |
| PHUSE EU |
2019 |
Navigating FDA Requirements: ISS/ISE Build Strategies |
Priyank Patel |
source |
9 |
| PharmaSUG |
2019 |
CBER Data Standards Update and BioCompute Progress |
Elaine Thompson |
source |
27 |
| PHUSE US |
2019 |
Data Harmonization Using Machine Learning [presentation] |
Lex Jansen |
source |
20 |
| PHUSE US |
2018 |
FDA CBER Data Standards Activity Update |
Lisa Lin |
source
presentation source |
4 |
| PharmaSUG |
2016 |
Moving from Data Collection to Data Visualization and Analytics: Leveraging CDISC SDTM Standards to Support Data Marts |
Steven R. Kirby,
Terek Peterson |
source |
8 |
| SGF |
2016 |
Finding the One: Using SAS Code and SAS Data Quality Server to Create a Matched Record |
Elena Shtern,
Kim Hare |
source |
25 |
| PharmaSUG CN |
2015 |
SAS End-to-End solutions in Clinical Trial |
Emma Liu |
|
17 |
| PHUSE EU |
2014 |
FDA Guidance on Standardised Study Data for Electronics Submissions |
Lauren L. Shinaberry,
Éanna Kiely |
source
presentation source |
7 |
| PHUSE EU |
2014 |
Risk based monitoring using integrated clinical development platform Authors |
Sita Rama Swamy Peddiboyina,
Shailesh Vijay Joshi |
source
presentation source |
9 |
| PHUSE EU |
2014 |
Update on Regulatory Guidance: Data Standardisation Planning for Clinical Development Programs |
James R. Johnson |
source
presentation source |
10 |
| PHUSE EU |
2013 |
Time Travel for Librarians: Versioning Complex Library Metadata for Past, Present or Future Retrieval |
Nico De Leeuw,
Ine Felsenstein |
source
presentation source |
12 |
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