Quality Assurance Blog Posts & Updates

10 Reasons Top Pharma Companies Automate Proofreading with GlobalVision’s ‘Verify’ Platform

Date: May, 2024 | Category: Proofreading | Author: Amanda De Luca In the highly regulated and complex world of pharmaceuticals, accuracy and precision are paramount. Even minor oversights or errors in labeling, packaging, or documentation…

Reduce Your Carbon Footprint & Boost Sustainability Through Automated Proofreading

Date: April, 2024 | Category: Proofreading | Author: Hana Trokic Automated Proofreading—A Sustainable Approach to Proofreading That Reduces Carbon Footprint in the European Union and Beyond The current global climate urges…

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A Guide to EU Pharma Regulatory Compliance: Everything You Need to Know

Date: April, 2024 | Category: Compliance | Author: Hana Trokic Understanding the complex regulatory compliance landscape of the European Union’s (EU) pharmaceutical industry poses a significant challenge for companies aiming to…

Company, Compliance, Featured, Proofreading, Quality

GVD Braille Height Sets A New Standard for Precision and Speed in Braille Inspections for EU Pharmaceutical Market

Date: April, 2024 | Category: Compliance | Author: Hana Trokic GlobalVision’s Braille Height is breaking new ground by offering unmatched precision and speed never before seen for regulatory Braille inspections. With the new GVD…

10 ChatGPT Prompts to Enhance Pharmaceutical Proofreading

Date: April, 2024 | Category: Proofreading | Author: Hana Trokic With AI, pharmaceutical companies can now streamline the process of analyzing vast amounts of data and documentation, ensuring compliance with regulatory standards…

Company, Featured, Proofreading, Quality

The Verify x Esko WebCenter Integration Automates Proofreading and Inspections for Packaging Artwork

Date: March, 2024 | Category: Proofreading | Author: Hana Trokic The Verify x Esko WebCenter Integration represents a digital shift in the packaging artwork review process. Verify x Esko WebCenter - An Integration to Unify Your…

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…

Company, Compliance, Proofreading, Quality

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 GVD Braille Module

Company, Compliance, Featured, Proofreading, Quality

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.

Compliance, Customers, Proofreading, Quality

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.

Compliance, Featured, Quality

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.

Featured, Quality

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.

Our cutting-edge technology brings unmatched accuracy and speed in proofreading of critical content, ensuring compliance success every step of the way. For Inova Pharma, it has allowed them to take full ownership of quality reviews and ensure seamless product launches as well.

Compliance, Customers, Proofreading, Quality

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.

Company, Featured, Proofreading, Quality

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.

Featured, Quality

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.

FDA Labeling Requirements Pillar Post Banner Image

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.

Compliance, Featured, Quality

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.

Proofreading, Quality

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.

Company, Proofreading, Quality

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.

Company, Customers, Quality

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.

Veeva Selects GlobalVision as a Silver Status Technology Partner

Company, Quality

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 File Comparison Tools

Proofreading, Quality

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…

Screenshot of GlobalVision Verify Features

Proofreading, Quality

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.

Recycle to avoid waste on the print production floor

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?