The number of test samples required for adequate lot-to-lot validation protocols is high and may be prohibitively large, especially for low-volume or complex assays. Monitoring of the distributions of patient results has the potential to detect lot-to-lot inconsistencies relatively quickly.
Read more:
Failure of Current Laboratory Protocols to Detect Lot-to-Lot Reagent Differences: Findings and Possible Solutions
Source: Clinical Chemistry
Art and Science of Laboratory Medicine
Facebook: www.facebook.com/LaboratoryEQAS
Twitter: LaboratoryEQAS
maintaining data integrety consistency , above Info. is correct !
ReplyDeleteHi, you make mind blowing ideas and a spectacular article here. Last time, when I saw your site this was a little good but today I visit the web site again and find that you guys making a very smart work on the site. Today Web surfing is run very fast and a huge competition over the web is spread. So it is quite interesting. Thanks…reagent
ReplyDeleteThank you Vendela
Delete