White Paper

White Paper: Stability Tests In Hot, Wet Climates - The Global Harmonization

Source: BINDER

Stability testing for pharmaceutical products has now been harmonized globally. All pharmaceutical products must undergo defined specific testing conditions in accordance to local climatic conditions.

With the ICH guideline Q1A (R2) for stability tests which was finalised in August 2003, and revised in 2005 (withdrawal of the chapter Q1F, which defines additional stress testing conditions in zones III and IV) new changes have taken place. With the withdrawal of chapter Q1F, the 10 member ASEAN countries have introduced their independent technical dossier related to the ICH guidelines and have adapted the testing conditions to suit their own climatic conditions. The enforcement of the ASEAN ICH guidelines into the ASEAN countries is currently in progress.

access the White Paper!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Bioprocess Online? Subscribe today.

Subscribe to Bioprocess Online X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.

or

Subscribe to Bioprocess Online