PRISYM ID will be exhibiting at the Clinical Trial Supply East Coast 2019 on the 16th and 17th of October, in King of Prussia, booth #16.
Over the two days, delegates and speakers will discuss new trends and opportunities and learn how they optimize their clinical supply chain enabling them to stay ahead of the game.
Simon Jones - VP of Global Products PRISYM ID will also host a Think Tank session on day 1 at 3:45 pm:
Managing the emerging industry challenges to your clinical trial supplies labeling and packaging
The forthcoming EU Clinical Trial Regulation introduces new challenges by requiring primary and secondary pack label updates to be performed (EU CTR EU No 536/2014 Annex VI). It is the latest industry change to cause many Clinical Trial Supplies teams to re-think their labeling processes.
- What is the current best-practice thinking for clinical trial labeling and packaging?
- Do new Supply chain models, such as Just in Time (JIT), offer sufficient benefits to justify their adoption?
- Which technologies and standards (eLabels, GS1, E Ink, etc) help ensure clinical labeling pro-cesses are both flexible and fit for purpose?
Our labeling 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 CTR EU No 536/2014 Annex VI 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 booth #16 for more information and to grab a copy of our Annex VI Infographic.
Are you Ready for The Annex VI EU No 536/2014 Labeling Changes?
