Kallik provides pharmaceutical manufacturers with a competitive advantage through offering an end-to-end labeling and artwork management solution which drives compliance with increasing pharmacovigilance and regulatory requirements. Our software enables robust traceability across manufacturer, provider, patient and regulator domains, releasing them from the constraints imposed by legacy and home grown labeling solutions.
Safe
Ensure comprehensive FDA and EU-compliant labeling to minimize the risk of counterfeit medicines entering the supply chain
Global
Implement flexible, standardized labeling strategies that de-risk entry into promising emerging markets
Digital
Accelerate adoption of ISO IDMP data model and alignment with EU Telematics requirements
Unified
Align product and package labeling with RIM, MDM, ERP and PLM systems to provide a single source of truth
Traceability
Full traceability and transparency over the life sciences supply chain with detailed audit trails of all actions
Automation
Minimize the risk of human errors, ensure compliance and improve efficiency with automated artwork and rules-based decision making
How Kallik Can Help Pharmaceutical Manufacturers
Kallik has a wealth of experience working with life sciences organizations and manufacturers. Our label and artwork management solution, Veraciti™ is continuously adapting to the changing requirements of the pharmaceutical industry. At Kallik, we work to ensure our customers needs’ are catered for while helping them achieve their business goals.
Veraciti is the only end-to-end labeling and artwork management software, meaning it supports the lifecycle of your organization’s labeling from the asset and phrase managers through to factory printing and distribution.
Compliant Artwork and Labeling
Pharmaceutical organizations operate within a highly regulated environment and are constantly facing changing regulatory requirements. Learn more about how Kallik can help pharmaceutical companies stay compliant with ongoing and future regulations here:
Check out our latest Pharmaceutical resources
Why New Medical Device Regulations Require More Than Ad-Hoc Manual Processes
This time around, products really do have to ‘do what they say on the tin’!
An Intelligent Approach to Labeling & Artwork
Using an intelligent rules engine helps organizations handle market challenges more efficiently
Do Your Customers Trust Your Label And Your Brand?
The steps organizations should take to ensure their labeling instils trust in their end consumers
Enterprise Labeling Management In Heavily-Regulated Industries: 5 Critical Success Factors
Five success factors for achieving the desired benefits of an end-to-end labeling management project
Fighting COVID-19 with Automated Labeling
How businesses can navigate the uncertainty of COVID-19 with remote, automated labeling capabilities
Maintaining Labeling Compliance In Highly Regulated Industries
The three areas businesses need to get right to ensure their labeling meets GxP requirements
Reducing Errors In Factory Print: The Case For Labeling Digitalization
It is too risky to leave the accuracy of market-facing product information to chance
UDI & Product Traceability For Medical Devices: White Paper
How a more strategic approach to labeling digitalization can better serve businesses & regulators
Establishing End-To-End Control Of Product Labeling
Five important drivers for building a global labeling strategy
Lessons & Leftover Challenges from MDR Preparations: What Next?
How medical device companies can effectively overcome the challenges posed by EU MDR
3 Ways Improving Your Labeling & Artwork Management Process Drives Speed To Market
In a rapidly changing regulatory world, how do you achieve speed to market?
2020 Statistics: The Benefits Of Automated Artwork & Labeling Have Never Been Clearer
Check out Kallik's highly impressive Veraciti™ user data from 2020
Remote Software Implementation: Lessons from the COVID-19 Pandemic
Going forward we’ll be introducing new tools that enable collaboration as though we were co-located
EU MDR Labeling Compliance - Are We There Yet?
Bob Tilling, VP Global Sales, explains how medical device manufacturers can recover lost time
How Companies Are Using New EU MDR Regulations To Improve Artwork & Labeling Processes
EU MDR forced changes on medical device manufacturers but has led to improvements in multiple areas
Why You Should Focus On System Design For Successful Software Implementation
We want our customers to realise the business benefits of using our solution as quickly as possible
Trust in the Cloud: The Value of AWS in Highly Regulated Industries
The value of using the cloud is clear: unrivalled security, and compliance are built in as standard
Change Management in Uncertainty
Listen to what your teams are telling you, and importantly, check-in with how they are feeling
Is Your Medical Device Organization On Track To Comply With EU MDR?
The clock is ticking on the need to ensure compliance with the EU Medical Device Regulation (EU MDR)
Why Can’t Labeling Be as Easy to Manage as Paying My Power Bill?
The best starting point: being willing to view and do things differently
What We Can Learn From EU Medical Device Regulation Compliance Preparations
MDR requirements alone should not determine how manufacturers overhaul their label management
The Transformative Power of Modular Content Generation
In pharma, labeling is critical to continued marketing authorization, confidence, and patient safety
Key EU MDR Changes You Need To Know About
New medical device regulations substantially change the ways manufacturers market devices in the EU
The Benefits of Applying Business Rules To Labeling In Highly Regulated Industries
The automation of manual tasks frees up resources, allowing you to attend to higher value activities
5 Ways to Make Your Supply Chain More Efficient
It is increasingly important your organization remains compliant when it comes to labeling
EU MDR: An Opportunity For Medical Device Manufacturers
Compliance is not a short-term business overhead, it is an opportunity to improve best practice
Why UDI Is Europe's Latest Hot Topic
Not only does data have value, but structured data has increased value
How Automated Labeling Can Help Your Organization Meet Strategic Goals
Some of the best streamlined approaches organizations can implement for long-term business benefits
Achieving Consistency Through Labeling Digitalization
Label digitalization builds an integrated, transparent supply chain for all involved in the process
Overcoming Aversion To Change When Adopting New Technologies
New systems can prove vital to the transformation to a more productive working environment
Document Versus Data: Why The Difference Matters
The difference between a document-oriented vs data-oriented way of managing your product information
Revitalize Highly Regulated Industries With Cloud-Based Labeling And Artwork Management
A lot of locked-in data needs to be released if we’re going to empower the new workforce
Simplifying Your Labeling Supply Chain
The steps that can be taken to simplify your labeling supply chain and the benefits this can deliver
Why Digital Labeling Is Crucial To Successful Digital Transformation
How to ‘digitally enable’ labeling and artwork processes
Labeling and the Art of Data Quality for UDI
How adopting best practice for managing labeling content can bring business value to UDI projects
How To Achieve Supply Chain Compliance
Discussing the need for transparency and visibility throughout the labeling process
Digital Labeling – A Business Rules Approach
Label digitalization enables robust regulatory submissions, increasing approval process transparency
How To Improve Return On Investment From UDI
The transition to UDI is a huge undertaking, so it is important companies take a wider perspective
Using Compliance Strategically To Enhance Business Processes
Compliance: why it matters and how you can see it as not just a necessity but a mother of invention
Integration Can Be Challenging, But We Need To Do It
If you don’t do integration right, you can't maximize the investment you made in enterprise software
Is Your Organization Worried About Product And Package Labeling?
Labeling and artwork management requires both transparency and visibility
Factory Printing: How To Reduce Errors, Accelerate Printing Times and Maintain Compliance
The risks of using manual processes for factory printing and how to successfully tackle them
Factory Labeling Migration Following Business Acquisition
Veraciti, with 21 CFR Part 11 electronic signatures, eliminated paper-based quality processes
Veraciti™ Sets New Quality Benchmarks at Integra LifeSciences
Surgical and medical instrument manufacturer Integra LifeSciences is a leader in medical technology
3 MDR Lessons Class II Should Learn From Class III Medical Device Businesses
Why it is vital medical device manufacturers begin planning a technology-led, long-term solution?
6 Steps Medical Device Manufacturers Must Take When Navigating The Digital Maturity Curve
For medical device manufacturers faced with tight regulations, manual processes are not feasible
How To Optimize Your Factory Printing Process
Manual processes leave factory printing vulnerable to countless errors, so how can this be avoided?
Helping Device Manufacturers Get Those Vital Ventilators Built
Delivering ventilators to the NHS on time with required labeling during the peak of the pandemic
How To Ensure Full IVDR Compliance On Time
A guide on how your company can get compliant with new medical device regulations
4 Key Actions To Ensure IVDR Compliance Deadlines Are Met
The next challenge after EU MDR is IVDR. Don't let your business fall short of compliance
Why Digital Maturity Is Essential For Medical Device Manufacturers
Digital maturity is paramount in highly regulated industries, and we’re going to explain why
Kallik At 20: Two Decades Of Innovation That Have Shaped Global Label & Artwork Management
What we've learned in 20 years of labeling & artwork management
Why Your Business Should Act Now To Be Compliant With IVDR
Why your business should act now to be compliant with IVDR
Kallik Brings Technology & Industry Expertise To Help Teleflex Deploy A Global Labeling System
How Kallik helped Teleflex revolutionize their labeling
Keep The Supply Chain Flowing With Truly End To End Integrated Digitization
How Kallik helped manufacturers overcome extensive operational challenges faced by businesses
How Managing The Simple Medical Device Label Could Make Or Break Nordic Expansion Ambitions For Man
How effectively managing the simple device label could be key to overcoming the challenges of entering the
The Advent of Better Software Application UX to Manage Critical Manufacturing Processes
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
The four trends set to disrupt highly regulated industries in 2023
Leading Orthopaedics Company Össur Overcomes IFU Management Challenges With Veraciti™ Solution
Overhauls legacy asset management systems and disjointed processes to improve global business operations an
The Power of Enterprise Labeling Software
Enhancing Compliance and Efficiency in Enterprise Labeling
Artwork Automation: The new generation of artwork management tools
Artwork automation is revolutionizing the way large enterprises create and update product labels
Trust in the Cloud: Data Security in Cloud-Based Software for Labeling and Artwork Management
Addressing misconceptions and concerns about the security and reliability of cloud technology when it comes
Advancing Labeling and Artwork Content Management: Insights from the Kallik and Teklynx Webinar
How Label Templates Improve the Sustainability of Your Labeling and Artwork Process
This blog explores the environmental impact of traditional labeling, and how adopting online, cloud-based,
Reducing Downtime and Maximizing ROI: What to Look For in a Labeling and Artwork Management System
Kallik’s Guide to Mastering Enterprise Labeling & Artwork in 2024
Your Next Step in Mastering LAM