LEVERAGE SAS TECHNOLOGY TO ENHANCE YOUR EFFICIENCY

We offer a comprehensive range of SAS® Programming Services tailored to your needs.

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

CLINOVO SAS® PROGRAMMING SERVICES

Analysis dataset

Tables, listings and figures

Patient profiles

CDISC SDTM and ADaM mapping

System validation

Documentation (Data Transfer Plan)

Ad hoc clinical data reports

Edit check programming

Dashboard reports

Report automation

Data transfers

Our local team members have 15 years of experience

in the clinical trial industry.

Pharmaceutical and Medical Device

100% staff SAS® certified

Experts in complex programming

Speakers at all major SAS® events

To supplement our local SAS® experts, we have an

offshore team of SAS® programmers to meet your

highest expectations on time and on budget.

2011

SAS GLOBAL FORUM BEST PAPER 2 FDA PANEL SUPPORT SAS BUSINESS PARTNER

SAS® PROGRAMMING

PROGRAM

Clinical Programming Statistical Programming

CDISC® Express: Open source CDISC conversion tool

NEAT: Faster data cleaning and query resolution

OQMS: Query Management System

Patient Profile: Comprehensive, on demand and easy-to-read patient data

SAS®-BASED SYSTEMS

1208 E. Arques Avenue # 114 Sunnyvale, CA, 94085

+1 800 987 6007 contact@clinovo.com