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1 Nov 2018
Serialization and Validation with rfxcel (Part 1 of 3)
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rfxcel
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US
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2018On CPHI since
Other Content from rfxcel (7)
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News FDA Approves rfxcel for Verification Router Service (VRS) Pilot
rfxcel, the global leader in supply chain compliance and serialization solutions, has been approved by the U.S. Food and Drug Administration (FDA) to conduct a pilot to extend the testing of the Verification Router Service (VRS) for saleable returns. -
Brochure Keys to a Successful Solution Implementation Effort
Get ready for your compliance and serialisation implementation project. Contact us today to learn more about our approach to successful solution implementation, serialisation, and our track and trace solutions. Email: [email protected] -
Whitepaper Seven Secrets of Serialization
Do you know what’s happening to your products out there in the global marketplace? That knowledge could be the difference between security and vulnerability for you and your customers. Traceability has become a key tool for quality improvement in several industries and is a vital weapon in the war against counterfeits. Your supply chain peers tell us that implementing and managing traceability or serialization software is one of their key concerns. It is indeed a challenge but by learning from their experience, and using an experienced vendor, it doesn’t have to be as difficult as you think. At rfxcel, we design software systems to handle supply chain traceability in fast-moving, highly regulated and fully validated environments like the pharmaceutical industry. In this short white paper, we’ll share some of our design philosophy and some practical things we’ve learned along the way during customer implementations. -
Whitepaper Winning the numbers game: countdown to complying with the serialization requirements of the Falsified Medicines Directive
The Falsified Medicines Directive’s (FMD) February 2019 deadline is fast approaching. Those who don’t serialize by this deadline will be unable to sell their products in Europe. The regulations set forth by the FMD state that every Marketing Authorization Holder (MAH) must upload serialization codes to the European Medicines Verification Organization. But serialization isn’t a straightforward numbers game, and not all solutions are created equal. rfxcel has provided this document to help you determine how you need to serialize and what you need out of your serialization partner. Serialization is a daunting, frustrating journey, but having the right solution and the right partner can make a world of difference. This document aims to help you: Understand the regulation identify the right partner for a serialisation solutionTake these actions
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