| PharmaSUG |
2025 |
A Little Bit of This and That: Use cases, implementation, and documentation when using multiple CDISC standards, CTs, and regulatory guidances in an SDTM study |
|
source |
14 |
| PharmaSUG |
2025 |
Guidance from the FDA authored "Submitting Patient-Reported Outcome Data in Cancer Clinical Trials" and recommendations for their implementation in study CDISC COA data. |
|
source |
14 |
| PharmaSUG |
2023 |
We Can Work it Out: Dos and Don-ts for Small Biotech and CRO NDA/BLA submission partnership |
Jiaan Illidge |
source |
8 |
| PHUSE US |
2019 |
The Last Time? Efficiently Scheduling the Pieces of Your Submission Deliverables |
Emily Canosa |
source
poster source |
5 |
| SESUG |
2017 |
Challenges and Solutions for Handling Re - screened Subjects in SDTM |
Paul Nguyen |
source |
6 |
| PharmaSUG |
2016 |
Prepare for Re-entry: Challenges and Solutions for Handling Re-screened Subjects in SDTM |
Paul Nguyen |
source |
5 |
| PharmaSUG |
2014 |
A Parameterized SAS Macro to Select an Appropriate Covariance Structure in Repeated Measures Data Analysis Using PROC MIXED |
Leela Aertker,
Paul Nguyen |
source |
3 |
| PharmaSUG |
2014 |
BreakOnWord: A Macro for Partitioning Long Text Strings at Natural Breaks |
Richard Addy |
source |
8 |
HOME
QUICK SEARCH
AUTHORS
KEYWORDS
HELP
BUGS