Swissmedic urges medical device manufacturers to review their post-market surveillance (PMS) documentation after finding major non-conformities in recent assessments. Learn more about compliance with MedDO requirements
Swissdamed
Swissdamed: key information and deadlines for manufacturers of medical devices
Swissmedic urges medical device manufacturers to review their post-market surveillance (PMS) documentation after finding major non-conformities in recent assessments. Learn more about compliance with MedDO requirements
Device registration in Switzerland: Swissdamed module is live
Swissmedic urges medical device manufacturers to review their post-market surveillance (PMS) documentation after finding major non-conformities in recent assessments. Learn more about compliance with MedDO requirements