RxSource Shares Advice on Optimizing the Labelling Processes

Click Here to Watch the Webinar


Date: February 23, 2021
Time: 9AM EST / 2PM GMT

For Clinical Trial Supply organizations, being fleet of foot is essential. The recent pandemic has seen additional pressures placed on the supply chain, as drug shortages and patient recruitment have proved problematic for many companies.

Rhys Evans, Senior Director of CTS and Global Supply at RxSource, presents a case study on how his team implemented a cloud-based label management solution rapidly to optimize the company’s demand-led secondary packaging and labelling services, allowing them to supply medicines faster.

RxSource implemented the PRISYM 360 platform in a matter of weeks and is able to produce labels, package and supply medicines in as little as 48 hours.

In this Webinar, RxSource and PRISYM ID explore the key areas to optimizing your labelling and packaging processes.



Rhys Evans 150x150 - RxSource Shares Advice on Optimizing Labelling ProcessesRhys Evans, Senior Director, CTS and Global Supply at RxSource
Rhys oversees the Commercial Team and strategic growth of clinical trial services for RxSource. Rhys has worked in the clinical trial services arena for over 8 years and has a passion for exploring ways to streamline the supply chain to accelerate patients’ access to medicines without compromising on quality. He has a PhD in Respiratory Pharmacology and a First-Class Honours Degree in Applied Physiology and Pharmacology. In addition to working for RxSource, Rhys is a member of the Global Clinical Supplies Group Committee.


Steve Ellison 150x150 - RxSource Shares Advice on Optimizing Labelling Processes

Steve Ellison, VP of Global Clinical Trials at PRISYM ID
Steve has spent over 24 years working with coding and labelling solutions and for the last five years, he has been promoting the PRISYM ID’s world-class labelling solutions. During his time with PRISYM ID, he has observed many changes within the life science industry including significant tightening of regulations, the challenges of globalization and the implementation of directives. He has successful working relationships with a diverse spectrum of market-leading companies in medical devices, pharmaceutical, healthcare and clinical trial sectors.


Click Here to Download the Case Study

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