|
Charl ● 2008-01-09 12:56 (6720 d 19:00 ago) Posting: # 1482 Views: 9,089 |
|
|
Dear all... Hope your holiday was great as mine, many happy returns ![]() I want to know to what extent the QA does checking? is it a full check for every single detial or just as simple as random readings? what is the profile of a QA? as you know or as "it is known as". regards Charl |
|
chidambarajoshi ★ Hyderabad-INDIA, 2008-01-09 13:11 (6720 d 18:45 ago) @ Charl Posting: # 1484 Views: 7,397 |
|
|
Dear Charl, ❝ I want to know to what extent the QA does checking? is it a full check Internal QC ( Which is a part of QA) does the detailed checking ie., Raw data, print data and electronic data, where as random is done by QA Regards, Joshi -- Edit: Standard quotes restored. [HS] — Best Regards Joshi |
|
chiragkhatri ★ India, 2008-01-10 10:27 (6719 d 21:29 ago) @ Charl Posting: # 1493 Views: 7,398 |
|
|
Dear Charl, Normally 20% of randomly selected batches is sufficient for QA check, rest responsibilities lies with the department and more on internal QC Regards Chirag |
|
chidambarajoshi ★ Hyderabad-INDIA, 2008-01-11 06:00 (6719 d 01:56 ago) @ chiragkhatri Posting: # 1505 Views: 7,389 |
|
|
Dear Charl, 20 % of data checking could be serailly or randomly selected according to interal SOPs Joshi — Best Regards Joshi |
|
Charl ● 2008-01-13 11:00 (6716 d 20:56 ago) @ chidambarajoshi Posting: # 1512 Views: 7,351 |
|
|
Dear Joshi & Chirag thanks for your input. am looking for more detialed procedures, or what are the SOPs for a QA and for QC.? that are established all around. Is there a guidance to QA QC pratice inspecific.? regards Charl |
|
chidambarajoshi ★ Hyderabad-INDIA, 2008-02-27 10:25 (6671 d 21:31 ago) @ Charl Posting: # 1635 Views: 7,248 |
|
|
Dear Charl, No guideline are availble. We need to look into individual regulatory guideline and design SOP's. As for QMS is concerned you can opt for ISO. Regards, Joshi — Best Regards Joshi |

