Strict laws and regulations apply in laboratories and the pharmaceutical industry. The industry where the ManualMaster story started in 1992. With tools to make the management of the (paper) management systems that were used at the time manageable, traceable and transparent. In the following decades, ManualMaster underwent significant further development, often in line with our customers’ wishes. This is noticeable to this day. Whether you need to comply with GxP, ISO 17025, ISO 15189 or other accreditation/certification, ManualMaster will help you demonstrate, validate and make all your processes available. Moreover, you can integrate ManualMaster directly with CAPA management, audit management and, for example, the Management of Change. As such, you create one system for quality assurance and continuous improvement.