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7 Reasons Why Pharma Needs Document Comparison Software for Regulatory Proofreading
Date: March, 2024 | Category: Proofreading | Author: Hana Trokic Why does pharma need document comparison software for their regulatory proofreading? For pharmaceutical companies, keeping documentation compliant with regulations…
Verify’s New AI-Powered OCR Feature Brings Unmatched Character-for-Character Inspections to Regulated Industries
Date: February, 2024 | Category: Company | Author: Hana Trokic Verify's New AI-Powered OCR Feature is Here! Verify, GlobalVision’s newest and most innovative cloud-based proofreading software, has just raised the bar for proofreading…
Why Regulatory Affairs Teams Need Document Comparison Software in 2024
Date: February, 2024 | Category: Proofreading | Author: Hana Trokic Why do regulatory affairs teams need document comparison software in 2024? For Regulatory Affairs, where adherence to strict compliance standards and efficient…
Medicine Packaging: Navigating Regulations in the UK
Over the years, requirements of medicine packaging have undergone significant changes, driven by advancements in technology, changes in consumer expectations and needs, and, most importantly, the ever-evolving stringent regulations imposed by regulatory agencies such as the MHRA.
Revolutionizing Braille Inspection: Introducing the Upgraded GVD Braille Module
From a quality control perspective, Braille Inspection and accuracy play an important role as Braille is mandatory on pharmaceutical packaging all across Europe, and is strongly recommended by the FDA in Western markets, while other regions such as the ASEAN markets are working to heighten inclusivity by implementing braille requirements on packaging as well.
Dempsey Corporation Transforms the Label Review Process with GlobalVision
After exploring various solutions on the market, Dempsey Corporation made the decision to incorporate GlobalVision into their quality control processes. to eliminate errors and fatigue caused by manual proofreading.
A Beginner’s Guide to Sustainable Packaging
While “going green” may be a proud point for many businesses in this day and age, in the world of packaging and design, it’s not necessarily going far enough. Instead, it’s all about being sustainable.
How Document Comparison Software Improves Customer Experiences and Builds Trust
Document comparison software is one of those powerful tools that helps ensure the accuracy of all products that go out to market – from the inside out! Read on to explore how document comparison software is pivotal in revolutionizing customer experiences and fostering trust and brand loyalty.
An Introduction to Automated Quality Control
Automated quality control technology like GlobalVision, help businesses get products to market faster without compromising quality. By automating manual tasks that would otherwise take hours to complete, this technology speeds up the entire quality control process and significantly cuts down proofreading time.
Upgrading Your Brand? Streamline Brand Transitions With Document Comparison Software
Upgrading your brand is a complete journey but document comparison software is a solution that makes it that much easier. Not only does it prevent content errors, but it also ensures a seamless transition to new typefaces by automating a good deal of the proofreading process.
Accelerating Success: GlobalVision Revolutionizes iNova Pharmaceutical’s Product Launches with Unmatched Accuracy and Speed
iNova Pharmaceuticals is a global organization dedicated to the development, marketing, and distribution of a diverse range of prescription medications and consumer health products.
Ready for a New Verify Release? 2023.2 is Here
With the latest Verify 2023.2 release, users can expect a heightened and more streamlined automated proofreading experience. This upgraded version comes equipped with new features and capabilities that not only enhance the user experience but also improve the accuracy and efficiency of quality inspections.
How GlobalVision Helps Hero Group Eliminate Human Error in Their Quality Control Process
Hero Spain decided to test GlobalVision’s inspection technology. The results of the inspections showed that it was very much possible to automatically proofread and inspect files with few false positives and in record time.
How to Master FDA Labeling Requirements: Your Comprehensive Guide is Here
This comprehensive guide provides detailed insights into FDA labeling requirements and ensures your organization not only thoroughly understands labeling guidelines, but also sets best practices in place to consistently meet FDA labeling requirements with complete ease.
RCount – The Next-Generation Automated Counting System
RCount by GlobalVision is the market-leading automated counting system and technology that ensures compliance and traceability of sensitive materials. Your teams can now count your critical assets with 100% accuracy in record time.
Your Complete Guide to Meeting FDA Labeling Requirements
FDA labeling requirements vary from market, product, and commodity. Each product, depending on its intention of use, has its own set of requirements that manufacturers need to follow.
How to Ace FDA Food Label Compliance Review: Ensure Your Labels are Always Approved
To ace FDA food label compliance reviews and ensure your labels are always approved, tap into the power of automation. Automated quality control is a comprehensive solution for your compliance needs that ensures all of your food labels meet FDA label compliance review.
Overcome Your Content Challenges in Cosmetic Labeling to Meet FDA Requirements
Cosmetic manufacturers operate in a highly regulated industry, further complicating the labeling process. Not only do they have to consider branding and marketing guidelines, but they also have to focus on FDA cosmetic labeling requirements, as there are strict rules and regulations behind every cosmetic label.
How to Ease the Labeling Proofreading Process for Medical Devices
A medical device can range from the simplest household item found in everyone’s pantry, like a band-aid, to more complex technology like an x-ray machine. Regardless of its complexity, there is a constant amongst them all. They all need to be tested and approved to meet FDA requirements and compliance.
Ensure Your Labels Meet all FDA Drug Labeling Requirements with Automated Quality Control
For highly regulated industries like pharmaceuticals, following FDA drug labeling requirements is one of the most crucial aspects of the product lifecycle.
Use Text Inspection Technology to Keep Up With Global Market Demands
Text inspection technology allows you to not only automate your workflows, but it also relieves the burden of having to rely on outdated methods and technology that will not let your business reach its full potential.
Don’t Miss The Proof – GlobalVision’s First Proofreading & Quality Control Digital Conference
We are extremely excited to announce that we are hosting an exclusive online event, specifically designed for proofreading and regulatory professionals in the Pharmaceutical, Life Sciences, and CPG industries. Our digital event will feature a variety of interactive sessions including Ask-an-Expert Q&A, a Fireside Chat, and expert sessions with speakers from our own GlobalVision team, Biogen, Alcon, Gilead, and more.
Our Biggest Release Yet. Verify 2022.2.
Verify is inspection technology reinvented—a web-based proofreading platform that ensures that you produce error-free content with the utmost ease, accuracy, and efficiency. With Verify’s automated proofreading solutions you can now streamline your work processes and produce higher-quality content in a fraction of the time.
You Don’t Want to Miss These Top 10 Pharmaceutical Conferences and Events in Fall 2022
After almost two years of virtual events, 2022 is bringing things back to how it was pre-COVID-19 pandemic. In-person events are once again in full swing, with live events being the greatest opportunity to grow and build networks and businesses, all the while learning about new trends and innovations in the pharmaceutical industry.
A Deep Dive into Enterprise Pharma’s Content Efficiency Problem
To avoid recalls caused by content errors, companies must inspect the artwork at every step of production, ensuring the accuracy of the text, labels, design, braille content, and barcodes. Innovations in automation now allow pharmaceutical companies to implement all-in-one quality control platforms like GlobalVision, that check text, spelling, artwork, graphics, braille, and barcodes at every stage of production.
How Johnson & Johnson’s Labeling Team Scaled their Quality Review Process
For over 20 years, GlobalVision has been helping Johnson & Johnson teams globally through the power of automation technology. Enabling automated quality checks throughout their packaging workflows is the backbone that has made this partnership so fruitful and successful. From the Consumer Health division to their internal Medical Device giant Ethicon, the nature of J&J’s regulated products makes the need for error-free packaging components an absolute necessity.
GlobalVision Advances to the Silver Certified Level of Veeva’s Technology Partner Program
Proofreading critical content accurately and at scale is a major concern in the Enterprise Pharma and life sciences industry though, currently, content and documentation checks are still mainly done manually. This is otherwise extremely tedious, time-consuming, and with a high margin for human error. Veeva, the leader in cloud-based software solutions for the life sciences industry, and a Veeva Technology partner, GlobalVision, together have found an answer to this problem— an end-to-end solution for regulated industries to scale the creation, review, and distribution of highly critical content.
Five Reasons Why You Should Use A File Comparison Tool
Date: March, 2022 | Category: Proofreading | Author: Hana Trokic Just as we become more dependent on technology with every passing day, businesses should also take note. Digital transformation is essential for any business that…
Verify 2021.4 – Annotating Files, A Deeper Look
Date: February, 2022 | Category: Company | Author: Hana Trokic Verify's Intended Changes Feature
Digital content creation is synonymous with the term 'revision.' As copy is being created, changes are constantly being made, resulting…
8 Strategic Techniques to Quickly Get Your New Product to Market
To be successful in a consumer-driven business, it’s essential to deliver quality, innovative products, and fast! Accelerating your new product’s time-to-market can help your brand become an industry leader and stand out from the competition.
How Automation Helps Manage Technical Writing & Symbols in Pharma
In the pharmaceutical and life sciences industry, any type of packaging error can lead to negative consequences for a company. Complete recalls could be needed, affecting the brand’s reputation and potentially resulting in lawsuits or damage to a patient’s health.
5 Ways to Optimize the Pharmaceutical Labeling Process
Product development and manufacturing are at the forefront of any pharmaceutical company’s business activities. Research and development, as well as product innovation help, are key factors in differentiating one company from another in the pharmaceutical landscape. In such a competitive and regulatory environment, a successful product market integration is essential to the success of your company.
How to Effectively Manage Print Samples with Automation
With so much competition between brands, packaging design is a key way to distinguish your company from others and thus persuade consumers to purchase your products. That is why brands must take great care to avoid little errors that can ruin a great packaging design.
Why Automated Quality Control is the Key to Getting Products to Market Faster
The modern business era has been characterized by a constant need to produce and deliver products with speed and efficiency. Long delays can result in financial losses and wasted resources that could have otherwise been used to acquire new business. Globalization and digitalization have redefined the standards of business practices by enabling companies to sell their products in various foreign markets. In turn, competition between brands has increased exponentially and companies are being held to the highest standards of customer satisfaction.
What are the Benefits of Implementing a Quality Inspection System?
If you’ve clicked on this article, chances are you’re considering implementing a quality inspection system in your organization. Maybe your business is losing money due to delays in the quality control department, maybe you’ve had a critical error slip by unnoticed, or maybe you just want to give your team the tools they need to get the job done more efficiently.
How to Avoid Waste on the Print Production Floor
From a business perspective, it makes sense to avoid waste whenever possible. Print waste in particular costs companies time and money, since any mistakes made during a print run will have to be corrected with additional resources. It’s more than just material waste — there’s also employee labor that must be factored in.
The Growing Role of Packaging in Building a Strong Brand Identity
When you think about your products, what sets them apart from others in the industry? Are they more durable than the competition? Do they have better features or a more user-friendly design? Why should customers choose you over another company?
Streamlining Pharmaceutical Artwork Management
Developing pharmaceutical packaging can feel as complicated and lengthy of a process as developing the product itself. If left without logical structure, this process quickly becomes vulnerable to inconsistencies and human limitations that can slow down workflows, cause unnecessary reworks, and put companies at risk of a recall.
How to Verify Digimarc Barcodes with GlobalVision
Date: March, 2020 | Category: quality| Author:Kayla Caticchio A new era of barcodes is here. With big-name retailers and consumer goods companies replacing traditional barcodes with Digimarc barcodes, printers are facing more challenges…
The Top Back-Up Strategies to Keep Data Integrity Intact
Date: August, 2019 | Category: quality | Author: Ryan Szporer “Just” backing up data isn’t enough to keep data intact anymore. While it’s a necessary step and a good start at that, a backup means little if there aren’t adequate…
Logical System Security as Crucial to Data Integrity as Physical Measures
Date: July, 2019 | Category: Quality | Author: Ryan Szporer
When you hear the word “security,” what comes to mind? Maybe you think of the stereotypical security measures that have crept into our collective consciousness as…
How Validation Leads to Data Consistency and Integrity
Date: June, 2019 | Category: Quality | Author: Ryan Szporer Consistency is a trademark of both validation and data integrity. In fact, without validation and the consistency for which it strives, forget data integrity. It’s like there…
3 Ways Error-Detection Software Ensures Data Integrity
Date: June, 2019 | Category: Quality | Author: Ryan Szporer There are many ways to ensure data integrity. As automation becomes increasingly prevalent in the 21st century, software, especially on the back end, is as important as…
Manual Proofreading Errors: How to Stop Label Recalls in Your Supply Chain
Date: April, 2019 | Category: Quality | Author: Mike Malz Regardless of the industry, all companies have the same goal in mind: to provide high-quality products to keep customers loyal and attract new ones. To accomplish this, each product…
The Key to a Successful Software Development Lifecycle? Data Integrity.
Date: January, 2019 | Category: quality | Author: Ryan Szporer In spite of the term Software Development Lifecycle (SDLC), there aren’t concrete steps to follow when coding. Each case is somewhat different, even if there is one universal…
The Importance of an Audit Trail to Securing Data Integrity
Date: January, 2019 | Category: Quality | Author: Ryan Szporer It’s easier to think of an audit trail as a collection of breadcrumbs leading out of the woods. The Bright Side of Being Audited Admittedly, the word “audit”…
Why Error-Free Packaging and Labeling Is a Must
Date: November, 2018 | Category: Proofreading | Author: Ryan Szporer Pristine, error-free packaging, and labeling undeniably look good, but it’s more than that. It’s a necessity, regardless of the industry in question. Of course, it…
What is a Quality Management System?
Date: August, 2018 | Category: Quality | Author: Marvin Magasura
What is a Quality Management System?
A quality management system (QMS) is a term that refers to a system in charge of documenting all processes, responsibilities,…
What Is “Quality Inspection”?
Date: July, 2018 | Category: Quality | Author: Marvin Magasura Terms like “audit” and “inspection” are prevalent in any manufacturing business. The first one refers to analyzing manufacturing organizations and processes, whereas…
You Can Always Get What You Want… in Packaging Quality Control
When it comes to packaging quality control, it’s not necessarily about catching every difference. It’s about catching every difference you want to.
GlobalVision is an intelligent inspection
platform that finds errors in your work
before they become problems.
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