Phil Johnson, Senior Principal, IQVIA Quality Compliance Medical Device and In Vitro Diagnostics (IVD) manufacturers have been busy the last few years ensuring that their Quality Management System (QMS) met the requirements of ISO 13485:2016 and the Medical Device Single Audit Program (MDSAP). It was an interesting time as Notified Bodies (NB) and certification bodies [...]The post Next on the MedTech QMS Calendar appeared first on Pilgrim Quality Solutions Blog | Quality Management Blog.