Bioequivalence and Bioavailability Forum

Main page Policy/Terms of Use Abbreviations Latest Posts

 Log-in |  Register |  Search

Back to the forum  Query: 2018-05-25 09:15 CEST (UTC+2h)
 
manusyriac
Junior

India,
2018-03-08 10:20

Posting: # 18505
Views: 424
 

 IP retention EU regulatory requirements [Regulatives / Guidelines]

Hi All,

I would like to seek your help in getting your thoughts on the EU regulatory requirements on the investigational medicinal product retention at sponsor manufacturing sites. Especially my focus area is the quantity of IP to be stored at manufacturing site.

Please guide me.

Regards
Manu
Back to the forum Activity
 Thread view
Bioequivalence and Bioavailability Forum | Admin contact
18,290 posts in 3,889 threads, 1,169 registered users;
16 users online (0 registered, 16 guests).

The purpose of models is not to fit the data,
but to sharpen the questions.    Samuel Karlin

The BIOEQUIVALENCE / BIOAVAILABILITY FORUM is hosted by
BEBAC Ing. Helmut Schütz
XHTML/CSS RSS Feed