Pharmaceutical Labeling

This time around, products really do have to ‘do what they say on the tin’!

Using an intelligent rules engine helps organizations handle market challenges more efficiently

The steps organizations should take to ensure their labeling instils trust in their end consumers

How a more strategic approach to labeling digitalization can better serve businesses & regulators

How medical device companies can effectively overcome the challenges posed by EU MDR

Five success factors for achieving the desired benefits of an end-to-end labeling management project

It is too risky to leave the accuracy of market-facing product information to chance

Five important drivers for building a global labeling strategy

The three areas businesses need to get right to ensure their labeling meets GxP requirements

How businesses can navigate the uncertainty of COVID-19 with remote, automated labeling capabilities

In a rapidly changing regulatory world, how do you achieve speed to market?

Check out Kallik's highly impressive Veraciti™ user data from 2020

Listen to what your teams are telling you, and importantly, check-in with how they are feeling

Bob Tilling, VP Global Sales, explains how medical device manufacturers can recover lost time

EU MDR forced changes on medical device manufacturers but has led to improvements in multiple areas

Going forward we’ll be introducing new tools that enable collaboration as though we were co-located

The value of using the cloud is clear: unrivalled security, and compliance are built in as standard

We want our customers to realise the business benefits of using our solution as quickly as possible

The clock is ticking on the need to ensure compliance with the EU Medical Device Regulation (EU MDR)

The best starting point: being willing to view and do things differently

MDR requirements alone should not determine how manufacturers overhaul their label management

In pharma, labeling is critical to continued marketing authorization, confidence, and patient safety

New medical device regulations substantially change the ways manufacturers market devices in the EU

The automation of manual tasks frees up resources, allowing you to attend to higher value activities

It is increasingly important your organization remains compliant when it comes to labeling

Compliance is not a short-term business overhead, it is an opportunity to improve best practice

A lot of locked-in data needs to be released if we’re going to empower the new workforce

New systems can prove vital to the transformation to a more productive working environment

Label digitalization enables robust regulatory submissions, increasing approval process transparency

The steps that can be taken to simplify your labeling supply chain and the benefits this can deliver

How to ‘digitally enable’ labeling and artwork processes

Discussing the need for transparency and visibility throughout the labeling process

Label digitalization builds an integrated, transparent supply chain for all involved in the process

Not only does data have value, but structured data has increased value

Some of the best streamlined approaches organizations can implement for long-term business benefits

How adopting best practice for managing labeling content can bring business value to UDI projects

The difference between a document-oriented vs data-oriented way of managing your product information

Labeling and artwork management requires both transparency and visibility

If you don’t do integration right, you can't maximize the investment you made in enterprise software

The transition to UDI is a huge undertaking, so it is important companies take a wider perspective

Compliance: why it matters and how you can see it as not just a necessity but a mother of invention

The risks of using manual processes for factory printing and how to successfully tackle them

Veraciti, with 21 CFR Part 11 electronic signatures, eliminated paper-based quality processes

Surgical and medical instrument manufacturer Integra LifeSciences is a leader in medical technology

Why it is vital medical device manufacturers begin planning a technology-led, long-term solution?

For medical device manufacturers faced with tight regulations, manual processes are not feasible

Manual processes leave factory printing vulnerable to countless errors, so how can this be avoided?

Delivering ventilators to the NHS on time with required labeling during the peak of the pandemic

A guide on how your company can get compliant with new medical device regulations

The next challenge after EU MDR is IVDR. Don't let your business fall short of compliance

Digital maturity is paramount in highly regulated industries, and we’re going to explain why

What we've learned in 20 years of labeling & artwork management

Why your business should act now to be compliant with IVDR

How Kallik helped Teleflex revolutionize their labeling

How Kallik helped manufacturers overcome extensive operational challenges faced by businesses

How effectively managing the simple device label could be key to overcoming the challenges of entering the

UX optimised label and artwork management (LAM) software is the next step to optimising manufacturing proce

The four trends set to disrupt highly regulated industries in 2023

Overhauls legacy asset management systems and disjointed processes to improve global business operations an

Enhancing Compliance and Efficiency in Enterprise Labeling

Artwork automation is revolutionizing the way large enterprises create and update product labels