Seminar on pharmaceutical ingredients, France
The programme features a review of current legislative and quality issues and the impact that these will have on pharmaceutical excipient manufacturers, marketers and end users. Topics to be covered include:
- implementation of pharmaceutical legislation in the EU;
- ICH (International Conference on Harmonisation) developments and their potential impact on excipients;
- review of recently published EMEA (European Medicines Agency) guidelines on genotoxic impurities;
- excipient regulatory framework update for Japan, Russia, China and Iran.For more information, please click
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