Sampling time [Design Issues]

posted by Durga – India, 2018-08-14 07:37 (928 d 01:16 ago) – Posting: # 19167
Views: 2,649

We need to check the molecule available PK profile of drug (absorption, distribution and elimination). we need to read the guidelines how many sampling time points need to be set at different phases as per above mentioned.

you need to check the metabolite pharmacological activity (if applicable)

bases on the formulation also. it is also very important.

Edit: Full quote removed. Please delete everything from the text of the original poster which is not necessary in understanding your answer; see also this post #5. Please follow the Forum’s Policy[Helmut]

Complete thread:

 Admin contact
21,357 posts in 4,459 threads, 1,492 registered users;
online 9 (0 registered, 9 guests [including 4 identified bots]).
Forum time: Saturday 07:54 CET (Europe/Vienna)

The way to do research is to attack the facts
at the point of greatest astonishment.    Celia Green

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