Bioequivalence and Bioavailability Forum • Retention samples

priyanka12345
☆

India,
2018-05-09 17:57
(2970 d 00:22 ago)

Posting: # 18758
Views: 3,870

Retention samples [Regulatives / Guidelines]

Dear All

As per FDA guidance for industry on Handling and Retention of BA and BE Testing Samples
the following is stated.

Because the Agency has limited experience with the retention and testing of non-solid oral
dosage forms, the Agency is unable to recommend an upper limit for the retention of non-solid
oral dosage forms at this time.

Can any one please let me know how much quantity is required as reserve samples for suspension.

Regards,
PRIYA

Edit: Guidance linked and subject line changed. Please don’t shout! [Helmut]

anky1212 ☆ India, 2018-05-31 15:29 (2948 d 02:49 ago) @ priyanka12345 Posting: # 18830 Views: 2,835	Retention samples Post reply
	Dear Priyanka, As per USFDA guidance, "The quantity of reserve samples should be sufficient to permit the Agency to perform five times all of the release tests required in the application or supplemental application. " Same need to follow. Edit: Guidance linked. [Helmut]