This webinar will start with a quick introduction and some definitions about impurities. The ICH Guidelines will be talked about, as will be other guidelines derived from them. The USP approach to impurities is then discussed, mentioning some specific challenges like DEG/EG in excipients and nitrosamines testing. The webinar will conclude by showing examples of how the product line PAI (Pharmaceutical Analytical) can complement the work with USP RS (Reference Standards) from impurities.
Webinar