design outputs 820.30d & iso 13485 § 7.3.4 (executive series #13)
Published 3 years ago • 2.1K plays • Length 3:32Download video MP4
Download video MP3
Similar videos
-
3:22
design inputs 820.30c & iso 13485 § 7.3.3 (executive series #12)
-
3:46
design planning 820.30b & iso 13485 § 7.3.2 (executive series #11)
-
4:31
risk management 820.30g & iso 13485 § 7.1, 7.3.3, & 7.3.9 (executive series #21)
-
3:29
design changes 820.30i & iso 13485 § 7.3.9 (executive series #18)
-
3:51
design review 820.30e & iso 13485 § 7.3.5 (executive series #14)
-
2:37
what is iso 13485?
-
1:07:55
medical device standards overview: iso13485
-
11:12
what is iso 13485?
-
3:47
design validation 820.30g & iso 13485 § 7.3.7 (executive series #16)
-
3:17
design transfer 820.30h & iso 13485 § 7.3.8 (executive series #17)
-
3:44
design controls 820.30 & iso 13485 § 7.3 (executive series #9)
-
3:14
quality system record 820.186 & iso 13485 § 4.2.5 (executive series #26)
-
3:09
internal communication iso 13485 § 5.5.3 (executive series #62)
-
5:23
understanding quality management systems - iso 13485 - clause 7.3 - design & development
-
4:30
parametric release iso 13485 § 7.5.6 & 7.5.7 (executive series #91)
-
3:31
design controls general requirements 820.30a & iso 13485 § 1 & 7.3.1 (executive series #10)
-
3:29
design verification 820.30f & iso 13485 § 7.3.6 (executive series #15)
-
3:34
medical device reportable 21 cfr 803 & iso 13485 § 8.2.2, 8.2.3 (executive series #54)
-
3:24
software validation 820.30g & iso 13485 § 4.1.6 & 7.3.7 (executive series #20)
-
2:51
handling 820.140 & iso 13485 § 4.2.3, 7.1, 7.5.11 (executive series #48)
-
3:14
distribution 820.160 & iso 13485 § 4.2.3, 7.1, 7.5.9.2 (executive series #50)