LEVERAGE TECHNOLOGY TO ENHANCE YOUR EFFICIENCY

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

SAS® is the most powerful programming language used in the clinical trial industry. We leverage SAS® technologies to provide neat statistical reporting and effective study monitoring systems. We create user-friendly, safe and compliant SAS®-based web applications that help our clients submitt clean and accurate clinical data to the FDA.

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 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

Our offshore business partner allows us to mobilize

an extensive pool 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: Smart discrepancy tracking

Patient Profile: Comprehensive and centralized patient data

SAS®-based systems

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

+1 800 987 6007 contact@clinovo.com