Getting a new device or process out of the box and into clinical use is difficult and time-consuming. Most labs don't have the knowledge or the manpower to efficiently install and validate new technology while maintaining quality and service standards for their existing business.
We design and supervise functional, clinical, and analytical validations of molecular devices and processes. WIth an eye to both CAP accreditation and New York licensure, PLC will create a validation plan that fits into to your existing business. We'll oversee your staff, training them and helping to prevent errors that waste time and money. We will also produce the scientific and regulatory documentation that gets your technology investment into productive clinical use.