Seminars & Conferences

UDI and the EU MDR: What You Need to Know to Comply

Date: Thursday, 16 November 2017,11:00 AM Eastern/4:00 PM GMT, 1 hour duration


Join medical device labeling and data experts from PRISYM ID and Reed Tech to learn about the UDI aspects of the new EU Medical Device Regulation (EU MDR) in this free webinar.

Bridging the Gap – How to be EU MDR Labeling Compliance Ready by Using the Lessons Learnt from UDI

Labeling Webinar Series - A Date with the Experts on Global Labeling Systems

Date: 20 July 2017, 4PM London / 11AM EDT


Join us for this 60-minute information packed webinar on ‘Bridging the Gap – How to be EU MDR Labeling Compliance Ready by Using the Lessons Learnt from UDI’ to discover why EU MDR will change the medical device labeling landscape globally and how to best meet the impending challenges.

Filling the Gap - How Digital Transformation should be embraced when Building your Next-Generation Labeling System

Labeling Webinar Series - A Date with the Experts on Global Labeling Systems

Date: Tuesday 27 June 2017, 4PM London Time / 11AM EDT


Label Compliance Challenges for Small and Medium Sized Medical Device Companies

Can the cloud help?

Date: Wednesday 5 April 2017, 11AM EDT / 4PM GMT

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When it comes to medical device labeling and traceability, the smallest companies have the same obligations and requirements as companies many times larger, but have to meet them with few resources and within the tightest of budgets. The size of the organization does not matter — the FDA and other regulatory bodies do not draw distinctions.

Mind the Gap! Labeling Experts share the 7 Steps of building a Global Labeling System and reducing the Validation effort

Labeling Webinar Series - A Date with the Experts on Global Labeling Systems  

Date: Thursday 26 January 2017, 4PM GMT / 11AM EDT
For many life sciences organizations, bridging the gap between an existing labeling system and implementing a global labeling solution as part of the supply chain can be a key concern. Businesses must find ways to overcome the challenges of global implementation, validation, label inspection, language management and label postponement, whilst managing time and costs. 

Future-Proofing your Clinical Trial Supply Chain

Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain?

Are you struggling to implement an on-demand packaging model, which still meets country-specific regulatory and language labeling requirements?

Using integrated vision to achieve 100% FDA compliance

Label End to End Tracking. Do you have it?

Labeling is an integral component within the medical device production process, with manufacturers needing to ensure products are correctly identified and branded in accordance with the FDA’s stringent regulations.

How The GUDID Was it?

Implementing and achieving UDI compliance – have the benefits of UDI outweighed the pain?

For the sake of patient safety, the ability to track and trace medical devices at a global level is paramount. In the last couple of years the fruition of the FDA’s UDI (Unique Device Identification) requirements - a single global regulation for uniquely pinpointing medical devices in the supply chain - has meant that all medical device companies trading in and to the USA must comply.

Local Language Labeling Delivered on a Global Scale

Global medical device and life sciences product labeling is a complex subject and an integral part of the supply chain. The landscape is varied in terms of the systems and processes employed in designing, populating and printing labels (including booklets, inserts and IFUs). To control labeling on a global scale a number of key functions need to be managed including:

Keeping Your Labeling System Ahead of the Curve

Labeling is one of the most comprehensive and impactful processes in any manufacturing organization; it not only drives patient safety but also affects product distribution and business revenue. Many businesses are not yet leveraging the true potential of their labeling system and so not realizing the downstream benefits of efficiency savings, productivity gains, increased compliance and reduced risk.

A Best Practice Guide to Clinical Trials Labeling

Now available for download. In this 60-minute, information-packed session, PRISYM ID explores the challenges involved in clinical trial local language labeling and country specific design.

Vision Inspection – Managing Label Defect Control

In this 50 minute webinar Steve Ellison and Conor O'Kelly present a best practice guide to achieving zero-defect labeling.

Achieving UDI Compliance – More Than Just a Label Change

In this 60 minute webinar Jay Crowley, Vice President of UDI Solutions and Services at USDM and Hal Plant from PRISYM ID present how you can best incorporate UDI into your overall quality, compliance and risk management strategy to not only drive UDI compliance but deliver significant productivity benefits.

Mind Your Language; Controlling Labeling on a Global Scale

Experts share advice on managing source data, local language labeling & country specific requirements

Boston Scientific Share Advice on Streamlining End-to-end Label Lifecycle Management

In this 60-minute, information-packed session, Boston Scientific and PRISYM ID explores the key areas to revolutionizing your labeling process

The GHS Countdown – Are You Prepared for the June 2015 deadline?

The clock is ticking: PRISYM ID advises how to best plan and implement the CLP Globally Harmonized System of Classification and Labelling of Chemicals (GHS) across your organisation efficiently ahead of the June 1st 2015 deadline for mixtures.

A Revolution in Label Lifecycle Management - Taking a 360° View

Experts from PRISYM ID explore the six key areas to revolutionize your labeling process.

Controlling Clinical Trials Labeling on a Global Scale

PRISYM ID Clinical Trials Labeling experts share their advice on how to manage source data, local language labeling and country specific requirements.

Label Production Under the Microscope

Experts from PRISYM ID Identify the Key Areas to Successful Label Management, Production and Verification

Tips for Implementing FDA UDI without Derailing Production

Experts from the FDA and GS1 Share Advice on Improving Patient Safety with Unique Device Identification without Throwing Your Organization Off Track

Going Global: Best Practices for Managing Evolving Labeling Requirements

Get Tips On How To Ensure Your Label Design, Approval, Management and Production Processes Are Securely Met On A Global Basis.

Dropping the Gavel on Counterfeit Drugs

Oracle Joins PRISYM ID to Dicsuss How to Combat Counterfeit Medical Supplies and Optimize Business Processes with Web-Based, Serialization-Ready Labeling.

PRISYM Design 6 Overview

Learn About the New Features in PRISYM Design 6, Our Easy-To-Use Software Package for Designing Labels Templates and Printing Them In-House

Ensuring FDA Compliance: The Essential Guide to FDA 21CFR Part 11

How Confident Would You Be That Your Labeling Processes Comply With 21 CFR Part 11? Discover 5 Key Areas To Ensure a Successful Label Validation Process.

The Compliance Crackdown: Guarding Against FDA Action

Experts from PRISYM ID Explore What Is Required For FDA 21 CFR Part 11 Compliance And How Best To Achieve It

Automotive Component Labeling: How NSK Uses Technology to Accelerate Just-In-Time Deliveries

This Webinar Takes a Behind-The-Scenes Look at The Technology That Has Supported NSK's Successful Elimination of Returned Deliveries Due To Documentation And Labeling Errors.