4.1.14 Participation in registers Estimated reading: 1 minute 124 views Authors Goal and purpose Reports should also be left to bodies that summarise treatment data and use it to gain insights into the effectiveness and safety of procedures, such as cancer registries. Only in this way can experience be gathered beyond the hospital itself and contribute to the improvement of hospital services. Confidentiality and data protection should be guaranteed.Collection and dissemination of data from all relevant sources with the aim of obtaining data for quality control and assessment. Provision of information to registers, comparative statistics, participation in "external quality assurance". Application Description of the process Risks Resources Material Time required Documentation Responsibility and qualification Notes and comments Applicable documents Validation documents Terms Attachments 4.1 Documentation - Previous 4.1.13 Classification systems Next - 4.1 Documentation 4.1.15 Tumour documentation
