Cost-effective and Practical Services
CSA Soliance partners with leading equipment manufacturers to provide validation (IQ/OQ/PQ) services for equipment, instrumentation and software. Pharmaceutical, biopharmaceutical and medical device companies must maintain validation programs that ensure their equipment is qualified for use. These programs are costly maintain in house, leading many companies to request this service from their equipment vendor. Packaging our services with your products allows you to expand your capabilities without committing the resources needed to stay abreast of FDA regulations and keep compliance documentation current.
We provide validation services directly to FDA-regulated companies, so our experience is first hand and consistent with industry expectations. Our field engineers are trained in GMP requirements and the FDA’s current thinking on validation. Our work has a proven history of satisfying our clients and FDA auditors.