PRISYM ID to Exhibit at the Clinical Trial Supply East Coast 2018
PRISYM ID will be exhibiting at the Clinical Trial Supply East Coast 2018 on the 16th and 17th of October, in King of Prussia, stand no 25.
Over the two days, delegates and speakers will discuss how to select forecasting and planning technology, how to reduce waste in clinical trials supplies, how to choose your packaging strategy, but we will also discover all the new technologies that will disrupt your clinical trials supplies.
As Labeling is an important part of the clinical trials supply among Manufacturing, Packaging, Logistics, Clinical Sites and Re-Supply; come to our stand no 25 to discuss your labeling strategy.
Simon Jones - VP of Global Products PRISYM ID will also host a round table about the Challenges in creating a fit-for-purpose clinical supply chain model, discussing how viable, is a JIT/On-Demand production; what are best practices for managing country specific regulatory label requirements; how should the requirements, design and approval processes work between trial sponsors, and their CRO and CSO partners; and if the clinical labeling initiatives, such as e-labeling and industry pictograms, offer significant benefits or unnecessary complexity.
Our labeling software solution, PRISYM 360, is designed in collaboration with PACT (Project Authoring for Clinical Trials) group. The solution helps the clinical trials organizations to meet the strictest compliance requirements and regulations, such as EU Annex 13 Label Requirements or Country Specific Requirements. The platform allows customers to create a fully integrated approach across the whole label life cycle, transforming labeling production and processes.
Come by Stand no 25 for more information and to grab a copy of our Clinical Trial brochure: