2.5.17 Reviewing the success of treatment Estimated reading: 1 minute 932 views Authors Goal and purpose The collection of findings from follow-up investigations, including their critical scientific evaluation, must be regulated. Regular reports on the measures should be prepared and forwarded to designated bodies (e.g. higher-level registers). The management must formally determine how and by whom the data is to be analysed as continuously as possible and with what effects. Adverse events or complications must be responded to in terms of "non-compliant results" Area of application Description of the Resources Risks Documentation Responsibility and qualification Notes and comments Applicable documents Literature Terms Attachments 2.5 Aftercare - Previous 2.5.16 Follow-up examination (aftercare and monitoring obligation)
