PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Revolutionizing Gene Therapy for Hemophilia B 11 Asia-Pacific · Hyderabad, India
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PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Optimizing R Add-On Package Management: Seamless Management from Download to Deployment PO01 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
From Query to Compliance: Leveraging Standards, Technology, and Agile for Efficient Health Authority Responses PO02 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Cloud Computing: The Next Frontier in Regulatory Submissions PO03 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Advancing Pharmacogenomics: Implementing SDTMIG-PGx v1.0 in SDTMIG v3.4 PO04 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Debugging the Relationship of NCI - CTCAE in Laboratory and Adverse Events Data PO05 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Trial Design Domain Automation PO06 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Improved Longitudinal Data Analysis: A Piecewise Linear Mixed Effect Modelling Approach PO07 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Navigating the Accelerating Clinical Trials Landscape in AI Age – A Junior Statistical Programming Perspective PO08 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Implementing the CDISC Library RESTful API in R: Automated Access to Metadata Repositories and Controlled Terminologies PO09 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025poster·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!
Optimization of Multiple Enrolment/Screening Records in Demographics as Collected (DC) PO10 Asia-Pacific · Hyderabad, India
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Key Guidelines, Tricks and Experiences for PMDA and Comparison with FDA and CDE Submissions 01 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Essential JSON Skills for Clinical Trial Programmers 02 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Submitting RWD: Where We Are and Where We Are Going 03 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Automating SAS Program Header Updates with Macros 04 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Prompt, Program, Submit: Generative AI for Faster SDTM, ADaM, and TLFs 05 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Deciphering Exposure-Response Analysis Datasets: A Programmer’s Perspective for Oncology Studies 06 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Data Not Missing at Random in PRO Analysis 07 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
My DIY Swiss Army Knife of SAS Procedures: A Macro Approach of Forging with My Favorite PROCs 08 North America · Cary, NC
PharmaSUG SDE2025presentation·NC·Emerging Technologies and Standards
Upcoming Changes to the SDTM and SDTMIG 09 North America · Cary, NC