Ensuring Success in Your Package Design

Patient centric design and patient engagement, including graphic comprehension and elemental usability, coupled with end-to-end product protection require a robust design and development process.

Impact of the EU Clinical Trials Regulation (CTR) No 536/2014

AUDIO: our panel of industry experts walk you through a PCI Clinical Services watercooler chat discussing all the changes, benefits and potential disadvantages that the new EU Clinical Trial Regulation No 536/2014 will bring

Best Practice on Setting Health-Based Cleaning Limits in a Multi-product CDMO Facility

The best practice for setting and using cleaning limits within a multi-product CDMO facility.

Optimizing IRT for Clinical Supply Management

WHITEPAPER: IRT systems can be a double-edged sword. Set up properly, it can make your clinical supply strategy a breeze to execute. Set up improperly, it can apply additional pressure and stress to a sponsor’s resupply execution

Water Cooler Chat: Clinical Trial Supplies in a Whole New World

AUDIO: 2020 has been a year that has delivered the world many challenges, the equilibrium has shifted and so many things are no longer as they should be. The Pharmaceutical Industry, like many others, has had to adjust to a “New Norm”

Water Cooler Chat Session: Australia: Bridge to Asia-Pacific Clinical Trials

AUDIO: Asia Pacific is a growing destination for conducting cost-effective clinical trials – between 2007 and 2018 trials in Asia constituted around 2

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Your bridge between life-changing therapies and patients