When manufacturing highly potent solid oral dosage forms, taking an effective approach to cleaning the equipment used is paramount. Manufacturing Chemist Editor Dr Kevin Robinson recently caught up with PCI Pharma Services process experts Ben Potter, Amala Alex and Richard Parry to learn more about cleaning validation and verification, the differences between the two … and why they’re so important.
Cleaning validation and verification in a high potent granulation suite
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CDMO insights: development and manufacture of a highly potent OSD product
Read moreIn today’s pharmaceutical landscape, contract development and manufacturing organisations (CDMOs) are ubiquitous. Prior to the CDMO boom in the 1990s, however, this wasn’t the case
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