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.
The company, who specialize in the ethical sourcing, packaging and delivery of medicines for Clinical Trials, Research & Development and Expanded Access Programs, implemented the PRISYM 360 platform in a matter of weeks. It now enables RxSource to produce labels, package and supply medicines in as little as 48 hours.
In this 60-minute, information-packed session, RxSource and PRISYM ID explore the key areas to optimizing your labelling and packaging processes.
Key Learning Objectives
- Understand how to be ‘validation ready’ with a cloud-based labelling platform, including a pre-validated pack with industry standard print processes
- Discover how to mitigate the complexity and risk involved in clinical labelling, making sure labels and booklets are fully compliant, while taking control of design and printing process in-house
- Ensure shorter lead times of drug delivery by streamlining process and using an automated labelling solution
- Find out how to build up a library of approved language translations and automatically apply regulatory rules and intelligence to label content.
Audience
SVP/VP/Director/Head or Manager of:
Quality
Regulatory
Operations - Clinical trials
Labeling
Clinical Trial Services
Clinical Trial Supplies
Supply Chain
Clinical Supply
Labeling and packaging
IS/IT
Manufacturing / Production
