Kallik in the press

Take a look at some of the coverage Kallik has achieved in key pharmaceutical and medical device industry press publications, where we share our expert labelling and artwork management insights.

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Claims substantiation in the nutraceutical industry

Neil Gleghorn explores how claims substantiation can allow all product labels using a specific claim can easily be traced and updated, reducing the risk of printing out of date claims.

Read the article on NBR

Rationalize Your Labeling Approach to Prepare for the EU MDRs

Kallik CEO, Neil Gleghorn spoke with Medical Device and Diagnostic Industry on how a joined-up, cloud-based labelling and artwork management solution can help medical device organisations prepare for regulatory changes.

Read the article on MDDI

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Brexit – deal or no deal for labelling?

What does the implication of Brexit mean for the pharma and medical device industries? Speculation is rife, but it is widely assumed that the Medical Healthcare products Regulatory Agency (MHRA) will take over either some, or all, of the duties that have been carried out by the European Medicines Agency (EMA).

Read the article on EPM

Labelling, compliance, and its ever-changing environment: How can the pharmaceutical industry keep up?

Graham Francis, channel marketing manager from Kallik discusses how pharmaceutical firms can keep up-to-date with labelling compliance.

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Labeling: Keeping Up with Compliance

Regulation is of paramount importance and a challenge to manufacturers every day. So, how can the industry overcome some of the biggest challenges it faces, embracing new technologies in order to empower workforces and allow the industry to move forward?

Read the article on PharmExec.com

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Overcoming cultural challenges in the workplace when adopting new technologies

Here, in this online exclusive, Kallik looks at the need for a change in work culture and implementing new systems and procedures to make a more productive workplace.

Read the article on EPM

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Enabling Cultural Change in Organizations

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 do they enable change?

Read the article on PharmExec.com

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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. Graham Francis, product marketing manager at Kallik, explains how data integrity should be a top priority when using new technologies in the pharmaceutical industry.

Read the article on EPM

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Labeling: Unlocking the Locked-In Data

Graham Francis looks at how increased levels of data integrity and the shift in pharma’s organizational culture impacts labeling.