We are also a Control System Integrators Association (CSIA) Certified Firm and very familiar with GAMP5 requirements. This strict certification and experience reflect our commitment to providing quality and excellence to the automation industry. Our engineering department has an established reputation for providing innovative solutions for complex applications while maintaining compliance with regulations throughout our history. All of our solutions are designed to comply with 21 CFR Part 11 requirements. We are also capable of implementing and realizing the benefits of process analytical technology (PAT) to increase efficiency.
The flexibility of our services allows us to assist in any or all aspects of the validation process. Our proven experience ensures that the design, implementation, operation and qualification efforts progress smoothly. Out project management team maintains oversight on all aspects from start to finish ensuring that project milestones are met within the budget and schedule. We have the automation experts on staff that will maintain ownership and provide as much or as little assistance as necessary to meet your goals throughout the project lifecycle.
Cross Company Process can support all your pharmaceutical and biotechnology automation needs. We offer both automation and validation services to ensure a successful and cost-effective project while providing the highest quality service with strictest confidentiality.