SAS® PROGRAMMING LEVERAGE SAS TECHNOLOGY TO ENHANCE YOUR EFFICIENCY SAS® is the indisputable leading programming platform in the clinical trial industry. We leverage SAS® technologies to monitor key study metrics and prepare your statistical submission to the FDA. We also use SAS® to create user-friendly, safe and compliant web applications to streamline data management and biostatistics processes.
CLINOVO SAS® EXPERTS
SAS®-BASED SYSTEMS
Our local team members have 15 years of experience in the clinical trial industry. Pharmaceutical and Medical Device
PROGRAM
CDISC® Express: Open source CDISC conversion tool NEAT: Faster data cleaning and query resolution
100% staff SAS® certified Experts in complex programming Speakers at all major SAS® events
OQMS: Query Management System Patient Profile: Comprehensive, on demand and easy-to-read patient data
To supplement our local SAS® experts, we have an offshore team of SAS® programmers to meet your highest expectations on time and on budget.
CLINOVO SAS® PROGRAMMING SERVICES We offer a comprehensive range of SAS® Programming Services tailored to your needs.
Clinical Programming
Statistical Programming
Documentation (Data Transfer Plan) Ad hoc clinical data reports Edit check programming Dashboard reports Report automation Data transfers
Analysis dataset Tables, listings and figures Patient profiles CDISC SDTM and ADaM mapping System validation
2011
SAS GLOBAL FORUM BEST PAPER 1208 E. Arques Avenue # 114 Sunnyvale, CA, 94085
2 FDA PANEL SUPPORT
SAS BUSINESS PARTNER +1 800 987 6007 contact@clinovo.com