Incurred sample reanalysis [Regulatives / Guidelines]

posted by sarada06884 – India, 2013-04-09 14:22 (4822 d 08:22 ago) – Posting: # 10381
Views: 18,886

Hi Helmut,

Incurred sample reanalysis has been suggested by USFDA but I would like to debate on this topic.

How are ISR samples different from subject samples? The answer would be they are in vivo samples and the QCs are in vitro samples. ISR samples are meant for demonstrating assay reproducibility. Based on this now my concern would be:
  1. When the whole validation has been done based on in vitro samples and when the results of these experiments have been accepted then why ISR again?
  2. When Long Term Matrix Stability of the drug and metabolites are proven taking invitro samples is proven and when the stability of such experiment is accepted then why ISR again?
  3. Even though the ISR samples are reanalysed they are analysed along with CCs and QCs which are invitro again!!!!
  4. What if ISR fails?? probably they have to ascertain the cause and go for the development of the method again?????
Please give me your views

Regards
Srinivas

Complete thread:

UA Flag
Activity
 Admin contact
23,655 posts in 4,993 threads, 1,571 registered users;
127 visitors (0 registered, 127 guests [including 21 identified bots]).
Forum time: 22:45 CEST (Europe/Vienna)

Scientists cannot simply hang their subjectivities
up on a hook outside the laboratory door.    Ruth Bleier

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5