blood sampling [Study Per­for­mance]

posted by Ohlbe – France, 2007-11-04 01:29 (6793 d 07:30 ago) – Posting: # 1275
Views: 26,922

Dear drdds,

No guideline that I know of.

❝ if yes, what precausions to be taken in analysis?


I would suggest to specify in your protocol when you will be using real sampling times and when you will use nominal sampling times (e.g. deviation of more than x minutes, or x minutes before a specific time point and y minutes after, or x % deviation from nominal...).

❝ and what should be collection time points in crossover period??


Stick to the nominal time point in the protocol. No adjustment based on the deviation in Period I.

Regards
Ohlbe

Complete thread:

UA Flag
Activity
 Admin contact
23,653 posts in 4,991 threads, 1,570 registered users;
204 visitors (0 registered, 204 guests [including 15 identified bots]).
Forum time: 09:59 CEST (Europe/Vienna)

In theory, there is no difference between theory and practice.
But, in practice, there is.    Jan L.A. van de Snepscheut

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