|Partnership is the key to a successful project and we can contribute to your
business success— We will assist you in any way to meet your needs.
We have assisted FDA-regulated pharmaceutical, medical device, and biologics
manufacturers in meeting GMP, GCP, and GLP documentation and requirements
through audits, document preparation, corrective action implementation,
training, and consultation. We also offer hands-on field execution of project
assignments. We provide compliance services for regulatory submissions and
FDA inspections. Finally, we have an excellent record developing effective
training. Our proven record of accomplishment is attributable to the knowledge
and experience of our uniquely qualified resident experts, senior staff, and
network of affiliates. Our work with major Fortune 500 companies has exposed us
to current trends and inspection practices, which allows us to present proactive
solutions to our clients. We are experienced in providing solutions to your
technical and strategic assignments.
Our continued involvement in significant projects in these industries has
been the result of our in-depth knowledge of all project phases, from assessment
through discussion/negotiation and implementation, all with a constant focus on
Quality Systems and compliance.
cGxP values its relationship with our clients. Our company philosophy is to
enter each relationship as a committed partner who provides the client with
value- added service while ensuring that their facilities and processes meet all
regulatory requirements. We are always in pursuit of excellence, and we have the
expertise and proven ability to meet this challenge.