In our GMP
News of 21 November we reported that ICH Q8
"Pharmaceutical Development" and ICH Q9 "Quality Risk
Management" were finalised. So the FDA, EMEA and the Japanese
medicines authority will incorporate these regulations into their national
legislation. Now you can download the document ICH Q8 from the Internet
since EMEA was the first organisation to publish it on its website. Click
here in
order to download the document.
Compiled by:
Oliver Schmidt
on behalf of ECA
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