Forthcoming Webinars

If you want to find out more about any aspect of Artwork Management from the comfort of your desk then join us for one of our 30-minute webinars from the list below.  If you missed a webinar, feel free to listen to a recorded version.

Future events to be added shortly - Thank you for your interest

Past Webinars


  • Quadruple your Global Labeling capacity by adopting AMS technology

     

    In the majority of businesses, the Labeling Departments have played, and are still playing, the Cinderella role – critical but overlooked and underfunded.

    Without accurate messaging and labeling on packaging, brands and businesses in the regulated sectors will not have any products to sell. A bold statement I know but products, however good they are, will not be allowed for sale in modern day markets without the correct and compliant labeling.

    Businesses that underestimate the critical role that accurate labeling and messaging plays in the success of their business today, ultimately pay a biggest price in production down-time, protracted lead-times, product relabeling and the dreaded product recalls. In addition to this is the ongoing day-to-day expenditure on internal resource and external vendors.

    For those who are questioning the validity of these opening paragraphs, the ROI webinar highlights the touch-points that labeling content and packaging artwork creation plays across the manufacture and distribution channels of any product marketed in a regulated sector and the positive impacts AMS technology has on;
    • Direct costs
    • Efficiency savings
    • Opportunity costs
    • Compliance costs

    All compelling reasons to invest 30-minutes of your time

    Click to join the 10am (GMT) webinar
    Click to join the 5pm (GMT) webinar


  • How to effectively connect the change and labelling processes

     

    In 4 steps improve Medical Device, Cosmetic, Nutrition, Chemical and Pharma Label process.

    The key to efficient labelling and artwork is closely connected to the selection, collaborating and control of all the content that needs to appear on the product packaging, labels and leaflets.
    By systematically involving regulatory experts, marketing personnel and packaging teams as change requests are refined, this ‘content’ can be accurately communicated to the artwork creation teams.

    • Overview of typical “disconnected process”
    • Why do we need to improve?
    • What are the benefits of a collaborative process and connected content?
    • How to start the change

     

    View Recording

     


  • Ensure correct UDI content appears on labelling

    – Linking UDI data back to everything else about the product

    A label has multiple different types of content of which UDI content is not only a legal responsibility but an important part of your data that needs to be correct, compliant and traceable. We believe that Label & Artwork Management systems are about managing data and eliminating points of failure. So how do you make sure the correct UDI data always appears on the correct artwork?

    During this webinar we look at:

    • – UDI – What you should already know
    • – Understanding the importance of correct data
    • – Reducing the risk of failure points
    • – What is on my label?
    • – Traceability of data & version control
    • – Audits, reports and printing

    Discover how you can:

    • – Increase safety without hampering speed to market
    • – Protect patients whilst ensuring brand consistency
    • – Reduce compliance complexity
    • – Make changes in seconds

    Plus: Experiences of two medical device manufacturers as they prepare for UDI compliance.

    View Recording


  • Conquer 5 Key Challenges of GHS/CLP compliance

    – Bringing transparency to the whole artwork & Labelling creation process.

    With the deadline just under 1-year away for compliance in Europe, businesses across a number of regulatory sectors need to be amending their labelling and packaging artworks to comply with the 1st June 2015 deadline.

    Although GHS is a voluntary agreement rather than a law, it has to be adopted through a suitable national or regional legal mechanism to ensure it becomes legally binding. That’s what the CLP Regulation does.

    The Kallik solution can provide global organisations with a single web-based platform for managing all label and packaging artwork creation.

    • – Bring transparency to the entire process
    • – Driving swift changes across the whole of your labelling collateral
    • – Delivering consistency and compliance
    • – Easily integrate with other regulatory solutions
    • – Achieve time reduction and cost effective results

    Join us online to find out how we can ensure a swift and seamless transition to CLP compliant labelling

    View recording


  • Taking a holistic approach to Factory Labelling & Artwork Management


    Join us for 30-minute webinar to explore the relationship between Factory Labelling and Packaging Artwork Creation and how a scaleable Artwork Management solution can provide complete transparency across every step of the labelling process from packaging artwork creation through the factory labelling lifecycle.

    The labelling content (text, translations, symbols and brand imagery) that appears on factory labelling is often the same as on the different packaging components. To drive consistency and ensure compliance, doesn’t it make perfect sense that both are managed together?

    View Recording


  • Make your Gift Pack labelling as easy as ABC…

    Gift packs are proving to be a popular and useful sales technique that both the market and consumers find increasingly attractive. But they are also a technique that can trap the unwary, labelling wise.

    Here’s the issue: your labelling was 100% correct for all the individual boxes of let’s say lipstick and mascara. You know, as you took great pains to set that up. But, did you remember to transfer the same 100% accurate and full description to the outside of your multiple-pack box?

    This webinar will take a look at how using a data-centric approach you can easily access a module that, with a couple of mouse clicks, can group labels for individual products into bigger set, allowing you to build Gift Pack content in seconds!

    View Recording


  • Eliminate Errors on Labels & Leaflets

    Getting your systems and data connected

    This webinar will examine how easily errors occur on labels and leaflets. We will debate how these errors occur and present how they can be avoided by ensuring all your systems are connected to the correct source of data, thereby avoiding recalls and costly label re-work. We’ll take a look at some best practices that other companies have successfully used to eradicate the problem.

    View Recording


  • Getting Product Labelling Right

    Join us for this timely webinar to discuss the labelling requirements in the beauty and personal care industry. Kallik’s Neil Gleghorn will present the main elements needed on a compliant label and explore the wider implications of non-compliance on cosmetic companies. Neil will also discuss why the artwork production is fraught with issues and specifically talk about the labeling challenges as outlined in the recent European regulation.

    View Recording


  • UDI compliance – how easy a transition is it?

    Making UDI act as a catalyst to improve all artwork and labelling processes

    Medical device manufacturers can turn new product identifier requirements to their competitive advantage if they treat them as an excuse to make bigger changes to the way they manage label creation. During this webinar we look at the new requirement, the broader impact on labelling and how by taking a wider perspective will help to justify the investment and provide a holistic approach to all your labelling needs. Presented by Kallik’s Neil Gleghorn, the webinar will also chart the experiences of two medical device manufacturers as they prepare for UDI compliance.

    View Recording


  • Driving changes directly into Packaging and Labelling Artwork

    A roadmap to automation

    80% to 95% of artwork requests managed by Pharmaceutical companies are in fact change requests to existing artworks. This presents a huge challenge as to how to manage and reduce the reaction time to these regulatory driven changes.

    This ‘Roadmap to Automation’ webinar will outline how to implement an automated artwork management system that drives changes directly into artwork, providing an evolutionary roadmap to take companies from a classic internal studio (or outsourced artwork environment) to state-of-the-art automated artwork generation in simple, manageable steps.

    View Recording


  • UDI compliance – how easy a transition is it?

    Making UDI act as a catalyst to improve all artwork and labelling processes

    Medical device manufacturers can turn new product identifier requirements to their competitive advantage if they treat them as an excuse to make bigger changes to the way they manage label creation. During this webinar we look at the new requirement, the broader impact on labelling and how by taking a wider perspective will help to justify the investment and provide a holistic approach to all your labelling needs. Presented by Kallik’s Neil Gleghorn, the webinar will also chart the experiences of two medical device manufacturers as they prepare for UDI compliance.

    View Recording


  • UDI compliance – how easy a transition is it?

    Making UDI act as a catalyst to improve all artwork and labelling processes

    Medical device manufacturers can turn new product identifier requirements to their competitive advantage if they treat them as an excuse to make bigger changes to the way they manage label creation. During this webinar we look at the new requirement, the broader impact on labelling and how by taking a wider perspective will help to justify the investment and provide a holistic approach to all your labelling needs. Presented by Kallik’s Neil Gleghorn, the webinar will also chart the experiences of two medical device manufacturers as they prepare for UDI compliance.

    View Recording


  • Kallik AMS360 PLM for Artwork

    Show how Kallik’s solutions work with PLM to deliver content control and seamless integration with Artwork Management and creation functions

    How the Innovation models in PLM can be extended into Kallik

    Explain how our Artwork Generation tools use the extended content model to generate packaging and labelling component artwork in seconds

    View Webinar Recording


  • Health Canada's Labelling and Packaging Regulations – understanding the new changes

    Drug labels including package leaflets and inserts are a primary vehicle of communicating important information to health professionals, patients and consumers about the safe and proper use of drugs.

    This 30-minute webinar, targeting both non-prescription and prescription drug makers, will explore the recent changes to Health Canada’s labelling and packaging guidelines.

    Presenting best-practice techniques to avoid recalls, we will discuss artwork and phrase asset management and how best to ensure a compliant and error-free product

    View Webinar Recording


  • Kallik AMS360 PLM for Artwork

    Join us for a 30-minute webinar to explore how our “Full scope” Artwork Management Solution (AMS) together with our Automated Artwork Generation solutions enhances the change order process and data captured into PLM with a full label content management and a connected artwork creation process.

    • – Show how Kallik’s solutions work with PLM to deliver content control and seamless integration with Artwork Management and creation functions
    • – How the Innovation models in PLM can be extended into Kallik
    • – Explain how our Artwork Generation tools use the extended content model to generate packaging and labelling component artwork in seconds

     
    View Webinar Recording


  • Driving complexity out of the Artwork Creation process

    Why is the Artwork Creation process so complex and how can you simplify it?
    This 30-minute webinar will take a look at the conventional Artwork Creation process and explore why it is so labour intensive and fraught with error. Focusing on the day-to-day issues typically experienced by labelling and artwork project managers we will expose the complexities from the myriad of stakeholders to the sheer volume of artwork changes and explore how adopting technology could help to eradicate them.

    (Includes Kalliks 6 key theme – Artwork Creation )

    View Webinar Recording


  • One step to Simplifying your Artwork Review processes – Combine Quality Inspection tools with Artwork Management

    As organisations strive to improve the efficiency and accuracy of their artwork review process, we pose some key questions. How confident are you that only changes you asked for have been made; how can you automate the inspection and verification of Braille; do you have full audit trail of who reviewed a document and when; how comprehensive is your version control; how confident are you in your goods inwards QA and the quality of labels supplied; got eSignatures and audits all wrapped up, seamlessly and quickly? This webinar will address these issues and more, guiding attendees through the key steps to achieving this must sought after efficiency and accuracy.

    View Webinar Recording


  • Labelling content collation

    The key to efficient labelling and artwork generation lies in the processes and tools surrounding the collaborating and control of all the content that has to appear on the final packaging and leaflets. Then importantly, this ‘content’ needs to be accurately communicated to the artwork creation teams. During this webinar, Kallik’s Neil Gleghorn a deeply experienced expert in labelling and artwork generation, will outline how to adopt a collaborative approach to change management, involving regulatory experts, marketing personnel and packaging teams as change requests are refined and how to achieve this in a smooth and transparent way using workflow.

    View Webinar Recording


  • The New Cosmetic Regulation Landscape – 3 Key Challenges to Getting Labelling Right

    Industry regulations, audit pressures and operating across global markets are just some of the influences that have increased complexities around product labelling. Cosmetics and chemicals companies are faced with growing consistency and compliance challenges – challenges that are set to increase as each new regulation takes hold. This webinar will take a look at typical current artwork and labelling practices, outline why the artwork production process is fraught with issues and discuss how to address the new labelling challenges highlighted in the Cosmetic regulation

    View Webinar Recording


  • Avoiding Regulatory Recalls Caused by Packaging and Labeling Errors

    In this Webinar we will focus on the implications of packaging errors in the Life Sciences sector (both Pharmaceutical and Medical Device) and how best practice procedures can ensure your organisation avoids packaging related product recalls while ensuring all regulatory standards are met. We will also look at common problems we see at many of the customer sites we visit and how they can be addressed to ensure the artwork assets used in your labelling and packaging are efficiently managed.

    View Webinar Recording


  • The New Cosmetic Regulation Landscape – 3 Key Challenges to Getting Labelling Right

    Industry regulations, audit pressures and operating across global markets are just some of the influences that have increased complexities around product labelling. Cosmetics and chemicals companies are faced with growing consistency and compliance challenges – challenges that are set to increase as each new regulation takes hold. This webinar will take a look at typical current artwork and labelling practices, outline why the artwork production process is fraught with issues and discuss how to address the new labelling challenges highlighted in the Cosmetic regulation.