Webcast recording now available.
With heightened scrutiny by regulators and patient advocacy groups about the potential presence of impurities and degradants in medicinal products, it is imperative to effectively manage moisture, as it is known to be the main cause of degradation leading to impurities in solid-dose formulations.
Moisture is the main cause of degradation leading to impurities in solid dose formulations. So it’s important to get a grip early in development.
Watch this webcast to learn how the role of core ingredient selection, manufacturing conditions, and on-dose packaging (film coating) helps to manage the impact of moisture in the dosage form.