|+1 800 987 6007||Contact | Career | Blog | News|
Our team of experts. Clinovo has established a network of proficient SAS® programmers, clinical data managers, medical writers, Computer System Validation (CSV) specialists and CDISC® experts whose technical skills are needed to design all or part of a solid clinical trial. Our team has over 20 years experience in biopharmaceutical, contract research industries, technology and software development industries.
Our involment in the clinical trial community.
Very High Proficiency in SAS® & Web Programming and Open Source Technology
Cutting edge SAS® Programming. All SAS® programmers are certified by the SAS&® Institute and are able to leverage all the SAS® suite of products.
Through sophisticated SAS® web applications, we enable you to deal with multiple and complex user interfaces and keep full control and oversight of your clinical studies. With our web applications you get:
Efficient Open Source Technology. We are early adopters of open source technologies. By developing open source software for clinical trials, we expand the access to clinical systems, for they require no license fees while keeping high clinical data quality and security.
First Class IT infrastructure for a company of our size
Our IT experts bring over 20 years experience in software and engineering. All our software systems provide the highest Data Transfer Security and an extended Control of System Access. Our clinical data staff carries out full audit of your clinical systems and protocols to identify and evaluate your needs. With Clinovo you get:
Certified Staff on EDC Platform Market Leaders
EDC is one of our key competencies. We are experienced with all major EDC platforms and are able to efficiently translate study protocols into the right EDC study design.