GxP-CC was founded in 2013 with the goal to support Pharmaceuticals, Medical Devices and Dental companies to overcome the challenges of regulatory requirements.
Our customers fulfill a vital role in the supply chain of products which have a quality of life effect on all of us as patients. Our goal is to support and optimize the processes & controls to assure a seamless integration between the scientific results, the regulatory requirements, and the technological applications.
As a professional service provider, we strive to always keep our team ready today for tomorrow’s challenges. Business disruption coming with new technological advances is no longer a question of “if,” but of “when.”
Based on our extensive knowledge of the Life Science industry we believe GxP-CC can offer you services to make your projects successful, cost-efficient and within the project, a timeline initially defined.
All of GxP-CC’s consultants have been working in the pharmaceutical and medical device industries for numerous projects and in some cases over 20 years.
Each member of our consultant team brings an individual and unique knowledge of the industry to our clients.
From start-to-finish, the strategy is considered and provided to all of the guidance and hands-on activities to deliver your project.
The company was founded by experienced and active experts in the Life Science industry and they created a broad range of services for validation and qualification to the pharmaceutical, medical device, and dental industries.
By taking advantage of this extensive experience in product development and regulatory affairs, GxP-CC is leading and helping companies to accelerate and develop validation/qualification strategies over all phases of the software and hardware lifecycles.