Batch Production Record and Device History Record Review and Quality Assessment to ensure compliance with DMF and DMR specifications
Compliance Key INC - Medical Device Training Jerry Dalfors Jerry Dalfors is Keynote Speaker at Compliance key Inc .He has extensive (40+ years) of business administration, consultative, technical and managerial experience in the development and manufacture of highly regulated biopharmaceutical products including injectables, biologics, medical devices and oral dosages. Webinar Id: LSHCJB002 12:30pm PT | 03:30pm ET 01/23/2018 Duration: 60 mins Overview Written procedures are to be established and followed for a time efficient and clear evidence of the quality related elements during the review and approval for release, including packaging and labeling, to determine compliance of the intermediates (FDA definition) and/or finis...