The detailed documentation needed to meet CAP and ISO 15189 requirements could conceivably require organization and storage of thousands of pages of procedures, policies, and work instructions. Managing this information manually while meeting requirements of regulatory agencies is time consuming and cumbersome requiring many hours to complete. Even then mistakes can be made that may make the organization vulnerable to regulatory findings which could result in lost revenue and damage to market place reputation.
MasterControl Clinical Lab JumpStart provides a solution for collecting, organizing, and reviewing all the documents required to meet CAP, ISO, and FDA requirements. It is specifically preconfigured according to regulatory standards and industry best practices to help organize and control SOPs, policies, work instructions, and other documents to meet document requirement needs for clinical laboratories. The software provides multiple simple routes for document collaboration, approval, and review. It is an affordable solution for organizations that can benefit from automating document control process.