management representative 820.20b & iso 13485 § 5.5.2 (executive series #3)
Published 3 years ago • 1.7K plays • Length 3:31Download video MP4
Download video MP3
Similar videos
-
3:19
management review 820.20c & iso 13485 § 5.6 (executive series #4)
-
3:11
customer focus iso 13485 § 5.2 (executive series #59)
-
3:09
internal communication iso 13485 § 5.5.3 (executive series #62)
-
3:09
quality planning 820.20d & iso 13485 § 5.4 (executive series #5)
-
26:44
iso 13485:2016 medical devices — quality management systems, episode #4
-
55:31
overview of iso 13485 - medical devices
-
1:20:03
iso 13485:2016 medical devices — quality management systems — requirements for regulatory purposes
-
3:14
quality system record 820.186 & iso 13485 § 4.2.5 (executive series #26)
-
3:34
organization 820.20b & iso 13485 § 5.1 & 5.5 (executive series #2)
-
2:52
quality policy 820.20a & iso 13485 § 5.3 (executive series #1)
-
3:29
quality system 21 cfr 820.5 & iso 13485 § 4.1.1 – 4.1.4 (executive series #57)
-
3:46
design planning 820.30b & iso 13485 § 7.3.2 (executive series #11)
-
3:09
quality system procedures 820.20e & iso 13485 § 4.2.1 & 4.2.2 (executive series #6)
-
3:33
device packaging 820.130 & iso 13485 § 7.5.1, 7.5.11 (executive series #47)
-
2:35
understanding quality management systems - iso 13485 - clause 5.6 - management review
-
2:51
handling 820.140 & iso 13485 § 4.2.3, 7.1, 7.5.11 (executive series #48)
-
10:29
md-qms management responsibility clause 5 of iso 13485:2016 | training on iso 13485:2016 |
-
3:52
outsourced processes iso 13485 § 4.1.5 (executive series #58)
-
3:46
corrections and removals 21 cfr 806 & iso 13485 § 8.3.3 (executive series #55)
-
3:21
contamination 820.70e & iso 13485 § 6.4.2, 7.5.2. (executive series #35)