Design Outputs 820.30d & ISO 13485 § 7.3.4 (Executive Series #13) Quality Systems Explained 3:32 3 years ago 2 181 Скачать Далее
Design Inputs 820.30c & ISO 13485 § 7.3.3 (Executive Series #12) Quality Systems Explained 3:22 3 years ago 2 244 Скачать Далее
Design Transfer 820.30h & ISO 13485 § 7.3.8 (Executive Series #17) Quality Systems Explained 3:17 3 years ago 2 687 Скачать Далее
Design Controls 820.30 & ISO 13485 § 7.3 (Executive Series #9) Quality Systems Explained 3:44 3 years ago 2 643 Скачать Далее
Design Planning 820.30b & ISO 13485 § 7.3.2 (Executive Series #11) Quality Systems Explained 3:46 3 years ago 1 447 Скачать Далее
Design Review 820.30e & ISO 13485 § 7.3.5 (Executive Series #14) Quality Systems Explained 3:51 3 years ago 1 304 Скачать Далее
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Design Verification 820.30f & ISO 13485 § 7.3.6 (Executive Series #15) Quality Systems Explained 3:29 3 years ago 2 861 Скачать Далее
Design Controls General Requirements 820.30a & ISO 13485 § 1 & 7.3.1 (Executive Series #10) Quality Systems Explained 3:31 3 years ago 1 545 Скачать Далее
How to you create a Design History File (DHF)? Medical Device Academy 1:15:28 1 year ago 3 691 Скачать Далее
Do you have instructions for your design inputs? Medical Device Academy 15:23 Streamed 1 year ago 503 Скачать Далее
Design Controls 101 and Implementation Best Practices - Galen Data Galen Data 59:10 2 years ago 1 994 Скачать Далее
21 CFR Part 830 - Design Outputs and Reviews Learnaboutgmp Online Training 2:34 7 years ago 242 Скачать Далее
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