Lead validation consulting firm for a multi-million dollar state of the art sterile
    manufacturing facility.

Establishing a compliance framework for an IT organization within a multi-national
    pharmaceutical company.

Developing a 5 year plan to meet the compliance needs of a clinical organization
    within a large biotechnology company.

Assisting both large and small companies in implementing 21 CFR Part 11.

Developing and implementing an Enterprise BPA (Business Process Automation)
    Portal to manage GxP processes.

These examples together explain our capabilities and how we can assist our clients. These examples may sound different, but in fact they reflect our mission statement. We believe in the so-called “technology compliance engineer” theory and we are nurturing, developing, implementing and perfecting it.

We invite you to follow the links on this page to explore our firm and the services we provide.

Our Mission: "To provide value added technology and compliance solutions to meet GMP, GCP or GLP needs of our clients”.