September 15, 2017 08:12 ET
TORONTO, ON--(Marketwired - September 15, 2017) - This webinar will share how highly potent APIs can be developed and manufactured into suitable drug dosage forms including; solid oral, non-sterile oral liquids and semi-solid creams and ointments whilst adhering to the highest quality standards. Attendees will learn about the complexities at each stage of the development lifecycle, from the earliest phase of First in Man (FiM) studies involving drug in capsule, moving through ongoing clinical development and process optimization of often complex formulations ultimately resulting in commercialization and global supply.
Join industry expert David O'Connell, Director of Scientific Affairs at PCI Pharma Services, for an informative session on Thursday, September 28, 2017 at 10am EDT (3pm BST/UK).
PCI provides industry leading services for the development and manufacture of multiple dosage forms containing potent Active Pharmaceutical Ingredients (API) utilizing state of the art technology within a specialist contained manufacturing facility. This facility utilizes fully contained engineering solutions eliminating the need for Personal Protective Equipment (PPE) whilst safely processing molecules with an OEL as low as 0.01µg/m3. Geometric scale-up provides a seamless service from preclinical to commercialization delivering speed to market.
For more information about this complimentary event, visit: Development Manufacture of HPAPI Drug Products throughout the Clinical Phases
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