Labelling digitalisation – the importance of consistency

When it comes to the medical devices supply chain, it can often seem to be made up of a series of isolated steps from product development through to the patient or healthcare provider. Labelling digitalisation across the supply chain therefore, can help build a more integrated, fully transparent supply chain for all involved in the…


What’s new on the Kallik website?

Here at Kallik we’ve been working hard to improve our website to make it easier and quicker for you to discover what you need to know If you class your organisation as a heavily regulated industry facing challenges with keeping your labelling compliant or simply being uncertain about current levels of compliance, then you might…



Overcoming cultural challenges in the workplace when adopting new technologies

Processes and routines are two things that could be considered essential within the workplace. They are necessary tools to keep workflow going, businesses progressing, and employees focused on a day-to-day basis. But are they enabling change? As important as it is to have recurring methods in place, the introduction of new systems and procedures can…


Labeling: Unlocking the Locked-In Data

It’s been widely acknowledged and accepted by leading thinkers in the pharma industry that, in comparison to other industries such as automotive and retail, it lacks the vital innovative and modern methods that are being encapsulated by the fourth industrial revolution, Industry 4.0. It is all too common-place in the industry to see high inventories,…


The Effect of New Technologies on Drug Development

The development of new technology is playing a pivotal role in the advancement of both patient autonomy and drug development. It’s a huge challenge for regulators to ensure drugs being manufactured are adhering to uniform standards of quality and safety. Graham Francis, Product Marketing Manager at Kallik, explains how data integrity should be a top…


UDIs and Traceability for Medical Devices

Last week’s UDIs and Traceability for Medical Devices conference in Amsterdam highlighted some of the key developments in UDI implementation and alignment across regulatory, supply chain and customer environments as we move one year closer to the EU MDR. We had the opportunity to hear from and engage with key speakers and delegates from some…


Digital Labelling – A Business Rules Approach

By Graham Francis, Channel Marketing Manager, Kallik Ltd. In my last blog I talked about how organisations today are experiencing unprecedented demands from regulatory authorities and consumers alike for product labelling to be made clearer and more informative. Forthcoming regulations (including the new EU MDR regulations coming into force May 2020) also require labelling content to…


‘The Next Big Thing’: Adopting a Business Rules Engine to Unshackle your Labelling Teams

By Graham Francis, Channel Marketing Manager, Kallik Ltd. As March approaches, there’s much that those working within heavily regulated industries need to be focusing on for the rest of the year to stay compliant, take cost out of supply chain operations and increase their speed to market. At Kallik, we spend a lot of time researching…


2018: The Year When Labelling Matures as a Board Level Topic?

Firstly, Kallik would like to wish all of its customers a very happy and prosperous New Year and would like to thank you for your continued business and support.  We would also like to extend our greetings to our technology partners and those who are seeking to transform their labelling and artwork processes going forward…