Life Sciences

Experience Where it’s Needed

We have been building software applications for the life sciences industry since 2001 and have completed a wide range of projects to high standards of quality and customer satisfaction.

We are not an ordinary company and we do not create ordinary results. Some of the things that set us apart are the quality of our developers, a fully audited manufacturing process and the company infrastructure required to create software for FDA regulated applications such as clinical trials and electronic health records.

Developing custom life sciences software that complies with FDA standards is a specific, provable, auditable set of skills, procedures and infrastructure that only a few custom software companies possess.

We have proven our capability through independent audits and we welcome you to visit us and conduct your own audit of our methodologies, capabilities, standard operating procedures and infrastructure.

Some examples of our work for clients in the life sciences industry are:

HITECH Act

Industry experts estimate that 60% of the medical software in use within the United States today is not compliant with HIPAA and FDA regulations.

The Health Information Technology for Economic and Clinical Health Act introduced in 2009 increases the enforcement of HIPAA and FDA regulations…

21 CFR Part 11

21 CFR Part 11 is the FDA Regulation that set the standards for Electronic Medical Data.

Part 820 defines the manufacturing process required for FDA regulated environments. Building software to FDA standards …

HIPAA

The Health Insurance Portability and Accountability Act protects the privacy of patient data.

Software that contains patient data is required to have specific features that protect this data from misuse…