Lead validation consulting firm for a multi-million
dollar state of the art sterile
Establishing a compliance framework for an IT
organization within a multi-national
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.
"To provide value added technology and compliance solutions to
meet GMP, GCP or GLP needs of our clients”.