Finding the right solution to address drug stability concerns associated with moisture, oxygen and volatile compounds is a continual challenge.
TORONTO, Ontario (PRWEB) August 04, 2020
Bottles have long been the pharmaceutical industry’s solution to controlling the moisture and oxygen exposure that can cause stability issues with tablets and capsules. For clinical trials, successful supply strategies rely largely on the ability to control stability issues associated with moisture, oxygen and reactive impurities. The same issues are also present in the development of more potent APIs, larger molecules and modified release profiles. Innovative and evolving dosage forms, such as chewable and disintegrating tablets, also face heightened stability challenges and problems with shelf life.
Finding the right solution to address drug stability concerns associated with moisture, oxygen and volatile compounds is a continual challenge. As traditional packaging options can be inefficient, there is a need for new and specialized active packaging solutions to address these growing stability issues, especially during clinical trials. Additionally, repetitive package design processes and drug reformulations from stability failures are costly and can delay product launches; improved package design tools and processes are also needed.
Join Laura Zurlinden, Director of Business Development for Clinical Services, PCI Pharma Services, Badre Hammond, VP Commercial Operations, Aptar CSP Technologies and Tommy Genetski, Associate Director of Key Accounts, Aptar CSP Technologies in a live webinar on Wednesday, August 26, 2020 at 11am EDT (4pm BST/UK).
For more information or to register for this event, visit Extend the Shelf-Life of Oral Solid Doses with Activ-Blister Solutions.
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