GlobalVision text inspection software
 
 
 
 

The latest release from GlobalVision gives desktop users the ability to run faster and more accurate inspections with enhanced Text & Spelling Inspection features. Along with optimized processing speeds and improved usability, Version 5.5 introduces a new add-on tool for the inspection of tobacco packaging.

Top New Features:

Increased Processing Speeds

The newest version features a standalone Spelling mode thread by processing spelling inspections in the GlobalVision executable rather than the Text inspection executable. This update optimizes processing speeds by up to 4x, allowing users to complete revision cycles in a shorter time frame. In addition, users now have the option to preload files for Text Inspection.

GlobalVision users have the option to preload files for Text Inspection

Less Pixelation when Zooming In

GlobalVision 5.5 also comes with improvements to the clarity of text displayed during Text and Spelling inspections. The area of a file to which users zoom in is now rasterized at a higher resolution, reducing the pixelation of the image in the Master/Sample panel.

Text Inspection Software Allows 800% Zoom with High Resolution to See Details

Updated Difference List for Text & Spelling

Pop-up menus now help users navigate differences by clearly displaying levels and comments during inspections. The handling of Spelling dictionaries has also been addressed to improve the accuracy of punctuation errors detected during Text Inspection.

GlobalVision Text and Spelling Inspection Found Differences between Master and Sample

Health Warning Inspection Tool for Tobacco Packaging

With health-information and warning requirements becoming more and more regulated, tobacco companies are taking greater steps to ensure they meet high industry standards when it comes to packaging. Released with version 5.5, the latest innovation from GlobalVision was developed to facilitate the inspection of health warnings and artwork on tobacco labels and cartons.

GlobalVision Text and Spelling Inspection found 6 repeats in the file

The Compulsory Packaging Information (CPI) Extractor comes as an add-on to GlobalVision’s flagship Print Inspection system. Designed for use at each stage in the production process, it automatically compares cartons or press sheets to approved files to flag differences and ensures compliance with industry standards before going to print. This allows tobacco manufacturers to get their products to market faster by double-verifying health warnings and artwork in one complete inspection cycle.

 

Additional Features:

  • Generate comprehensive inspection reports to record and review all detected differences.
  • Stay on top of compliance standards by keeping track of each inspection with e-signatures for enhanced security.
  • Get color-coded grades of 1D and 2D barcodes in seconds without the need for a scanner with Barcode Inspection mode.

GlobalVision 5.5 is now available. To upgrade, contact sales.


Additional updates by GV: GlobalVision Desktop 5.7

Processes of proofreading, from marketing to print

Date: May, 2019 | CategoryProofreading Author: Ryan Szporer


It’s easy to imagine how much work goes into the production of packaging materials.

The Packaging Proofing Process

Even looking at the process in a vacuum, the back-and-forth alone in trying to finalize a design may spark images of heated boardroom debates on details as seemingly trivial as font size. However, before the packaging even gets to that point, it may shock you just how many steps are involved, in developing it from its infancy.

That’s not even taking into account factors like cost-effectiveness (including Return On Investment), time to market, and, perhaps most importantly, quality (accuracy). They all contribute to determining the degree of success of given packaging.

In effect, it’s a company-wide process of finalizing packaging (along with what’s inside), one that starts at the very top. Considering the financial ramifications of a mistake making its way onto the final product, it arguably stops there too, with one constant throughout the workflow being the need for thorough quality control.

Packaging Proofing in Pharma

Take a hypothetical company in the heavily regulated pharmaceutical industry, for example. Headquarters coordinates the launch of new drugs. And, while drugs themselves will likely be produced and packaged at different sites, the individual branding elements that go into the design are most probably determined at the head office. In effect, headquarters doesn’t just coordinate the supply chain, but all the different departments, including, in this case, marketing.

Input may come from the marketing units of offices around the world. It simply makes sense that they would get the chance to offer their two cents, especially with regard to packaging that will differ from one region to the next. Some of the content will nevertheless stay universal. Aside from the obvious elements (product name and branding), that content will take the form of drug and dosage information, for example.

In pharma, the Food and Drug Administration is the American regulatory body responsible, and documentation, like drug applications, has to be approved. A given firm’s Regulatory Affairs (RA) department liaises with the FDA, all the while reviewing packaging and labeling to ensure accuracy. It’s one of the first stages at which proofing becomes critical, to prevent typos and reduce back and forth. Truth be told, it’s just one of many product-development considerations with which RA helps, acting as a sort of bridge between departments.

The Reality of Conversion Errors

For example, with the approved copy (as well as technical and corporate-defined design requirements) in hand, the graphics or creative department begins to develop the file. The process is fairly intensive with a fair amount of artwork-creation checklist items for which to account, including making the file as accessible as possible to all other departments.

On that subject, even IT enters the fray, albeit indirectly. IT may not have any work to do with regard to the creation process, but the department is responsible for ensuring the homogeneity of software and platforms across the organization wherever possible.

The risk of conversion errors sneaking in at some point must be addressed. While it’s almost impossible to protect against the printer introducing them once the files get sent over, it’s relatively easy to ensure nothing of the sort occurs in-house simply by standardizing so that the files stay the same when being opened on different systems in each of the departments.

After all, to successfully determine whether the printer’s proof and subsequent shipment of packaging components match what had been approved internally, first, you have to make sure the file that had been approved internally actually appears as it should.

Approving Printed Packaging Materials

From there, it’s a matter of the internal quality control department proofing the shipment from the printer, ideally through proper sampling. The approved packaging then moves to production and gets distributed, ultimately landing in the hands of consumers. At that point, the packaging technically undergoes one final quality check.

Once the threat of expensive, required recalls or reprints dissipates, the quality objective can be safely confirmed to have been met. Assuming an efficient revision process, which can similarly be enhanced with the right digital proofing system, had been leveraged, so can the other two.

The trick is being able to sign off with confidence on the packaging before it even gets to that stage, though. It’s not so much a matter of bypassing the customer as it is of truly ensuring its quality for them and mitigating any risk ahead of time. Many different departments may be at work here, but proper proofing helps keep the operation running smoothly, limiting the number of revisions in play and ultimately the number of errors that slip through the cracks.

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Get your complete guide to meeting FDA labeling requirements here

Take the first step towards error-free packaging and labels by starting your free trial of GlobalVision

Learn how some of the world’s top pharma companies have cracked the efficiency code with automation

Cartoon computer work on the digital inspection fast and efficient comparing to manual work

Date: April, 2019 | CategoryQuality 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 must go through a strict proofreading process to ensure the accuracy of all labeling and packaging.

This can be time-consuming. As a result, some early adopters have switched to proofreading software due to time constraints. In fact, sticking with human proofreaders has proven to be a potentially costly mistake, one that may even lead to expensive recalls.

Avoid Manual Errors

Although they do their best, human proofreaders are not able to catch all errors that can be found on a label. In a North Carolina State University article about errors in food manufacturing, 25% to 50% of recalls were due to human error. There are many reasons why these errors were missed; For one, a proofreader could have been tired or simply unfocused.

With new technologies continuously introduced into every aspect of our lives, people can be distracted by an email alert or text message. When an error is detected in packaging, companies must issue a recall on their product, costing them thousands of dollars and leaving them with a ton of unsellable inventory. Fortunately, there are measures to ensure each packaging component is error-free. These measures can be combined into a single solution: an automated proofreading platform.

Proofreading That Checks Every Word

Human brains are trained to skip words. So, no matter how fluent they are in a language, they can overlook one that’s misspelled. Most people use spell-checking software such as the spellcheck feature in Microsoft Word or maybe even an online solution like Grammarly. These tools help catch those mistakes, but they do have flaws. For example, some English words are spelled differently, such as “color” and “colour.” One solution would be proofreading software that automatically detects errors in a loaded file.

Catch Discrepancies in Color

Despite evidence to the contrary, some may argue human proofreaders do catch misspelled words. Nevertheless, color differences are a different kind of animal. It’s important that the labels of packaging have a consistent color pattern. This helps promote brand awareness and identity. If the color has faded or the hue is slightly different, the product will come off as rushed. Color-detection software is one way to identify any issues before the file gets sent to the printing press.

A+ Barcode Grading

Every company wants to send out Grade “A” barcodes and nothing less, as recalls can be issued if they will not scan. And, yet, despite the very real need, human proofreaders are unable to tell if a barcode will scan properly when it reaches the customer. Leveraging technology is the only option here, and it makes sense to opt for the best solution possible. Having a process in place to digitally check barcodes saves you time and money. This is especially true when it comes to consumer goods.

Checking Labels Even After Printing

There is still a chance some errors or color differences will slip through the cracks even after the job is done and the labels are printed. The best way to review your printed files is by reverifying them, using proofreading software. This way the user can find any differences and decide to reprint if necessary.

It’s important to make sure that, even when the final label is produced, it remains error-free. It would be infinitely preferable to find errors in labels immediately after they’ve been printed instead of having a customer find them while in line at a store.

Making sure your products are high-quality extends to the packaging. Errors are not only costly but embarrassing. People are far from infallible, and companies that rely on human proofreaders risk having their products recalled and losing customers.

Making the switch to automated proofreading, like with GlobalVision, can save you time and money by sparing your firm from having to issue recalls. Businesses should consider spending a little more money now on solutions that help maintain their reputation and brand integrity. It’s not about short-term gains, but rather the long game, in which everyone is a winner.

_________________________________________________________________________________________

Get your complete guide to meeting FDA labeling requirements here

Take the first step towards error-free packaging and labels by starting your free trial of GlobalVision

Learn how some of the world’s top pharma companies have cracked the efficiency code with automation

Illustration of the FDA regulatory compliance process

Date: April, 2019 | CategoryCompliance Author: Ryan Szporer


 
 

There’s a saying: “Winning isn’t everything; It’s the only thing.” In business, however, before you can win, you have to first comply with regulations.

Sure there are get-rich-quick schemes that have earned many a matchstick man a pretty penny. Lasting success, though? That’s earned on the basis of hard work and a solid reputation.

This concept makes regulations the building blocks of any kind of fruitful venture. The rungs in a ladder or the linchpin in a wheel, if you will. The metaphors are especially apt because, when it comes to manufacturing consumable goods, regulations become the guiding force to all aspects of production.

The Key to FDA 21 CFR Part 11 Compliance

If success is built on a solid reputation, then reputation is almost like currency. Waste enough goodwill by taking customers for granted, or worse, for a ride, and you run the risk of having nothing left. That’s why abiding by guidelines is crucial for both your customers and business prospects. The Food and Drug Administration’s (FDA) 21 Code of Federal Regulations (CFR) Part 11 serves as a prime example of the lengths to which one must go to ensure compliance.

The set of guidelines applies to food and beverage companies, drug makers, and medical-device manufacturers among others, all of which are overseen by the FDA. The standards call for the implementation of various controls with regard to the processing of electronic data.

Requirements for the following controls are included:

  • Audits
  • Audit trails
  • System validations

Furthermore, and perhaps most notably, the subject of electronic signatures is covered in great detail. As electronic signatures become more prevalent, their legal weight has grown. They are now recognized throughout most of the United States as being just as binding as handwritten ones, possessing even greater security.

Following FDA Regulatory Compliance

FDA 21 CFR Part 11 effectively smoothed any company’s transition to digital records and electronic signatures at the time of its introduction in the 1990s by establishing international standards for each. Today, compliance keeps operational costs down and speeds up time to market, all by minimizing the risk of human error. Following set FDA standards is in the best interest of all parties involved, including the companies themselves who only stand to benefit.

The kinds of companies in question face a bevy of additional regulations. There are countless FDA guidances aimed at current Good Manufacturing Practices so pharmaceutical companies aren’t limited to respecting FDA 21 CFR Part 11.

For further proof, consider labeling and packaging, covered in 21 CFR Part 211. After all, even the smallest typos can have significant repercussions if dosage information is misprinted.

It all goes back to human error and how it must be mitigated, even if only to avoid costly recalls, with the well-being of consumers logically being an even higher priority. What should CEOs be more worried about? How much does a recall cost or how much damage a lawsuit can do? The first leads to significant short-term losses. The second leads to irreparable harm to a company’s brand equity and integrity to the point that there may not even be a long term.

The Real Building Blocks of Success

Systems do exist that both help eliminate the risk of human error and enable FDA 21 CFR Part 11 compliance. For example, the GlobalVision quality control platform, which digitally and efficiently proofs packaging components, has the required technical controls built into the software.

These include:

  • The ability to sign electronically, as mentioned earlier
  • A hierarchy of access levels, including managers and administrators
  • Inspection profiles only admins or managers can create or edit
  • A Login Management module, requiring unique User ID and password combinations
  • A comprehensive Audit Trail, which logs events, tracing them back to specific users

It’s critical to note software doesn’t ensure compliance. That is and always will be the responsibility of the manufacturer, but the right tools to make it simpler to get there. Just consider them building blocks in their own right, towards keeping compliant.

_________________________________________________________________________________________

Get your complete guide to meeting FDA labeling requirements here

Take the first step towards error-free packaging and labels by starting your free trial of GlobalVision

Learn how some of the world’s top pharma companies have cracked the efficiency code with automation

team working on text, color and graphics inspection

Date: April, 2019 | CategoryProofreading Author: Mike Malz


In spite of a whole industry dedicated to it, very few people know what prepress is. “Prepress” is used in the printing industry to refer to all of a commercial printer’s activities after they receive an order and corresponding graphics from a client, but before the actual job begins.

When you produce a business card, magazine, or any type of artwork and send it to a printer, the prepress department takes charge of checking it to make sure it’s ready to be printed without any issues, such as color distortions or size-related problems.

Modern prepress and reprographic professionals usually separate their duties into three stages which we will look into in detail in this blog post. 

Stage 1: Pre-Flighting

The first stage in the prepress process begins right after the graphics file is created and sent to print. During pre-flighting, trained and experienced technicians make sure the file contains all the necessary elements to undergo a successful print run.

For instance, graphics are checked to ensure the images have the proper resolution and format, the Pantone Matching System/CMYK color is set up, all the fonts are included, and all layout elements like crop marks, bleeds, and margins are also arranged.

Often prepress professionals, depending on the software used to create it, will need to convert the original file to a more printing-friendly format, such as PDF.

Put simply, pre-flighting is a crucial step where potential printing issues are caught early in the process. However, the vast majority of prepress technicians won’t find or correct any grammar or spelling mistakes, so it’s recommended that designers and clients run the file through proofreading and other quality control software before sending it to the printer.

Stage 2: Creating a Proof

Once the graphics file is approved in the first stage, it’s ready to move on to the second prepress stage – creating a proof. A proof is a close representation of how the finished work will appear when it gets printed.

In most projects, such as postcards or business cards, proofs are usually created in PDF format. Since PDFs are electronic files, they can be emailed to clients for quick and speedy approval.

The main purpose of the second stage is to ensure both printer professionals and clients are in complete agreement on what will be the desired outcome. Also, if your project involves any type of finishing operations like folding or binding – like with brochures or books – a physical proof is often created. This helps demonstrate how the final work will be constructed, the order of its pages, where it will be folded, etc.

Stage 3 – Printing Plates (in Case of Offset Prepress)

If the job requires a digital printing press, then the prepress work is basically over. The graphics file is electronically sent directly to the press without the need to create printing plates.

Although modern commercial printing facilities are shifting more and more towards digital printing, many companies still use the same tried-and-true offset method that has been the gold standard in the industry for over a century.

If the project is sent to an offset press, it requires the creation of printing plates the moment it is approved at the second stage. Printing plates are made from plastic, rubber, metal, paper, and other materials. Their main purpose is to properly transfer images to cardboard, paper, or other substances, and this is achieved using photomechanical, photochemical, or laser processes to engrave the image on the printing plate.

At this point, the actual run begins, bringing an end to the prepress process. From there, the printer lets the press do its job, verifying that the quality stays consistent throughout the run, before sending the shipment to the client. Both then and upon receipt, an additional quality control stage, or sampling, is required to ensure the client is being delivered exactly what they asked. Again, digital proofreading software becomes invaluable here, but it’s only a single key component of the prepress process, which, as a whole, sets the stage for a successful print run.

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Ensure your content is always error-free in record time with GlobalVision. Try it now for free. 

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Pills bottles with similar packages

Date: April, 2019 | CategoryProofreading Author: Ryan Szporer


 
 
 

While counterfeiting is usually associated with money, actual consumer products can be copied too, right down to the packaging. It’s an issue about which brand companies are ever-vigilant, leading to the development of several key anti-counterfeiting measures.

The Need for Anti-Counterfeit Measures

If you’re skeptical of the threat counterfeiting poses, consider the number of fake pieces of clothing or copied versions of video games and movies to which you may have been exposed. Indeed, counterfeit products are all over the place and readily available to most. However, the seriousness of the issue really should hit home when you think about goods like drugs and electronics, the latter of which, when counterfeited, tend to fail fire-safety tests.

Counterfeiting doesn’t just have negative ramifications for the victimized companies, but the consumers themselves. In fact, as just alluded to, sometimes the ramifications to consumers are much worse.

It’s true that, in the specific case of counterfeited non-consumables, purchases are often made by customers who know full well what they’re buying, as surveys have revealed. In such instances, consumers willingly sacrifice quality for a lower price point. However, fake products like pharmaceuticals, which actually represent the biggest piece of the pie for counterfeiters overall, are generally sold with the intent of being passed off as genuine articles. All it does is prompt more of a need for the previously mentioned anti-counterfeiting measures.

Covert vs. Overt Anti-Counterfeiting Measures

Measures run the gamut from Radio-Frequency Identification (RFID) tags for tracking purposes to anti-tampering technologies that similarly help to protect brand equity, just in a different way. The packaging design itself can be manufactured in such a way to make it incredibly hard for counterfeiters to replicate. For example, holograms not only add an aesthetic element but, if created using electron beam lithographic technology, can be near-impossible to copy.

Optimally, anti-counterfeiters must strike the right balance between the obvious (overt) and subtle (covert). While covert features are intended to help companies stay a few steps ahead of counterfeiters, overt features are meant to signal to consumers that the product is legitimate.

Covert features are meant to be hard to detect and copy. Overt features are hard to copy as well, though. Think along the lines of an anti-counterfeit sticker, which, when removed from the packaging, leaves visible damaging. Packaging that doesn’t have the sticker or a clearly identifiable spot where it was should be interpreted as a signal to the consumer to consider the product counterfeit as a precaution.

An Ongoing Battle Against Counterfeiters

Unfortunately, as ingenious as some of these measures seem, any advantage companies have in the ongoing high-stakes battle has to be seen as a stop-gap. Counterfeiters aren’t going to stop and in many ways, they’re winning in spite of the resistance.

In 2016, the cross-border counterfeit market was estimated as exceeding $1.7 trillion in cost, including indirect losses to governments and consumers. The compound annual growth rate from then until 2022 is meanwhile projected to be two to three times that of food, beverage, and pharmaceutical products.

In other words, there’s a lot left to lose. As proof, brand companies have already lost a lot, and not just in terms of the up-to 50% in revenue. Significant amounts of money are also spent by companies and governments, seizing fakes and developing future anti-counterfeiting strategies.

That’s why, in addition to developing effective measures that are irreproducible, cost-effectiveness is also a focal point. It may seem logical to include more anti-counterfeiting measures on the packaging that are required, following a better-safe-than-sorry mindset. Fewer is better here though, as long as the up to three recommended, visible elements are strong on their own. The proposed limit also makes it easier to inspect the packaging for potential tampering.

Furthermore, anti-counterfeiting elements need to be updated regularly. Companies would only be making their lives costlier and more complicated by needlessly overdoing it. It’s more effective to devote any excess financial resources to regularly updating the few elements you do have and making them as hard to replicate as possible than simply throwing a bunch of half-cooked eggs in the same basket at once.

Customer Communication Is Key

Similarly, when presented with the dilemma of whether to apply the same elements across all packaging and product lines or different ones, it’s actually better to go with the same ones.

Anti-counterfeiting experts Libor Šustr and Dr. Petr Hampl write in a Packaging Europe article published by Tim Sykes: “Because unit costs correlate with batch size, it is better to cover all products with the same element and make frequent changes. The advantage over potential counterfeiters is thus ensured and customer communication is easier.”

The customer communication point is key. It’s true that, if someone wants to buy a knock-off, they’ll find a way. In such an instance, it’s more of a customer loyalty issue than a counterfeiting one, where companies should be asking themselves why people want lower-quality versions of their products. It may make more sense to focus on improving your product if possible to the point that customers don’t want any cheap substitutes.

Anti-counterfeiting measures can only do so much, but they’re at their most effective when companies are working in conjunction with their customers. In the case of a counterfeit product that is designed to dupe consumers seeking authentic articles, like pharmaceuticals, you want to educate your customers to know when they’re getting what they want, i.e., your product.

It’s downright logical once you think about it, with anti-counterfeiting measures on packaging being proven to increase revenues in such an instance. Ultimately, it turns out, it is about money, specifically how to protect your investments, the most valuable of which is a company’s relationship with its customers. There’s just no substitute.

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Ensure your content is always error-free in record time with GlobalVision. Try it now for free. 

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Cartoon women standing with FDA icon and check mark

Date: March, 2019 | CategoryCompliance Author: Ryan Szporer


 
 

Of note, the Food and Drug Administration (FDA) has official data integrity guidelines, out in full force as we speak. However, firms who are already following current Good Manufacturing Practices (cGMP) have nothing to worry about.

Of course, the title of the document in question, “Data Integrity and Compliance With Drug CGMP”, serves as clear confirmation to that effect. It also somewhat formalizes cGMP as its own set of guidelines, but it’s best to consider what that acronym stands for before overreacting and realizing good manufacturing practices as a concept just makes sense.

Meanwhile, data integrity in this instance is simply a byproduct of cGMP, but achieving it is just as critical if not more so in this day and age.

Data Integrity and Security

Take for instance how compliance with the General Data Protection Regulation, or GDPR, is an ever-present item on the task lists of firms in the European Union these days. The security of customer data has become more critical in the internet age and data security and integrity simply go hand in hand.

For the uninitiated, data integrity, as defined in the FDA document, is “the completeness, consistency, and accuracy of data.” To achieve integrity, data should follow the ALCOA mnemonic device by being Attributable, Legible, Contemporaneously recorded, Original, and Accurate. Based on the official set of guidelines, abiding by many if not all of these should be downright logical.

For example:

  • Personnel should be trained to prevent and detect data integrity issues.
  • Each detected quality issue must be handled formally.
  • Only authorized personnel must have the necessary access to change records.
  • Each user should have their own, as opposed to shared, login credentials.
  • Electronic signatures over handwritten ones are permitted.

The Benefits of Good Manufacturing Practices

So, if these guidelines should already be in place, in conjunction with the proper operating procedures of any self-respecting company, why have them at all?

Well, it’s always better to make standards and regulations official. In an industry like pharma where skirting rules can have severe consequences for consumers, the need is even more prevalent.

In fact, the whole concept of cGMP originated from an inability to get fatal, contaminated tablets off the market in time, before they caused hundreds of injuries/ deaths in 1940. The FDA has multiple tools at its disposal these days to prevent such a disaster from reoccurring: random inspections, official warnings, and drug seizures. Arguably the most effective tool at all though is having the data integrity guidelines in place to start, because they’re preventative instead of reactive.

Keeping Up with FDA Regulations

Complying with cGMP admittedly means devoting a lot of resources to one’s operations. For example, appropriate quality management systems and procedures must be maintained, only qualified and fully trained employees must be kept on board, and reliable testing facilities and calibrated equipment must be used. What all those prerequisites have in common is they have come to characterize businesses serious about maintaining some semblance of long-term success.

While the abstract concept of data integrity is far removed from the drugs themselves, there is a direct relationship between it and product quality. Meanwhile, not only is there an indirect relationship between data integrity and product defects, but data integrity and product costs too.

So, in the end, the FDA isn’t asking firms to do anything other than to make life easier for themselves. After all, the “current” in cGMP simply seeks to remind companies that their systems must stay up to date with today’s latest technologies. Any company stuck in the past generally and justifiably gets passed by anyway. The overall goal may be to ensure customers don’t get hurt, but, if companies take the guidelines in stride, neither will they.

_________________________________________________________________________________________

Get your complete guide to meeting FDA labeling requirements here

Take the first step towards error-free packaging and labels by starting your free trial of GlobalVision

Learn how some of the world’s top pharma companies have cracked the efficiency code with automation

The invention of the printing press is often understated in terms of its importance, with the advent of the digital age in which we now live.

Date: March, 2019 | CategoryProofreading Author: Ryan Szporer


The invention of the printing press is often understated in terms of its importance, with the advent of the digital age in which we now live.

It’s true that these days, people can go entire days without reading something that’s been printed out thanks to the internet. However, not only has “digital” actually come to define an entire sub-sector within the printing industry, but, without the press, which promoted widespread literacy, who knows where we would be right now? Not to mention how it’s not just literature and collateral that gets printed out, but images and patterns on textiles that people use every day in the real world.

That digital sub-sector is also growing, and growing rapidly, with the implication being that rumors of the demise of the printing industry have been greatly overstated. And “digital” is but one method of man that printers use, with each of the below having their own unique applications. From letterpress to digital, here are the most popular printing methods today:

Letterpress Printing Method

Also known as typographic printing, letterpress dates back to Johannes Gutenburg’s 15th-century invention of the printing press. While the process, which involves hard-pressing an inked surface with elevated letters and images onto a substrate (printing surface), is one of the oldest available, it still remains prominent within the printing industry.

Two types of letterpress machines are the most common nowadays. For one, flatbed cylinder presses, on which the substrate is placed on a traditionally horizontal surface while a revolving cylinder applies pressure and makes the print, are renowned for operating slowly and topping out at 5,000 impressions per hour.

The other, the rotary press, features a master on one cylinder and a printing surface that is pulled between it and a second once the process starts. Able to make 20,000 to 30,000 impressions per hour, the rotary press is in the process of usurping the flatbed in terms of popularity.

Flexography Printing Method

Essentially an offshoot of letterpress, flexography is a form of relief printing that specializes in labels on cans and boxes. Presses run at high speeds and are typically very versatile, able to print cartons and labels on a variety of substrates on the same machine.

Plates, which form the print information and transfer the ink to the substrate, are made of rubber, making the process a relatively inexpensive one used primarily for short runs. The rubber plate wraps around a cylinder and picks up ink that will ultimately be deposited on the substrate. The flip side is that, unfortunately, the plates are very fragile and need to be replaced often.

Gravure Printing Method

Gravure printing is essentially the opposite of letterpress. The design to be printed is etched instead of elevated on a metallic master. The individual “cells” that are created contain the ink. Deeper cells result in darker tones.

Gravure tends to be more of an expensive process relative to flexography and is best suited for longer runs. Like flexography, gravure is common for packaging jobs within the packaging. Cylinders last significantly longer though. That’s one of several benefits, including consistent, high-quality results achieved with fast-drying ink that rivals the high-speed process itself.

Offset Lithography Printing Method

Offset lithography is a planographic printing process. So, whereas letterpress image areas are elevated and gravure image areas are recessed, they are on the same plane as the non-image areas for offset. Here, image and non-image areas are chemically separated.

The “offset” in the name refers to the presence of a third cylinder in the process besides the plate and impression ones. So, instead of the ink being directly applied from the master as it is with other methods, a rubber blanket serves as an intermediary between those cylinders.

Offset, which specializes in printing paper products like inserts and leaflets, is one method of choice in industries like pharma, in part because pharmaceutical collateral and packaging components call for fewer colors. For example, a typical press features multiple printing units, each devoted to a single color for one side of the printer. So, a single-color press has one unit, while a press with four units prints in cyan, magenta, yellow, and black (CMYK).

To print on both sides you can wait until the first has finished and the ink has dried before flipping the job over and restarting. You also have the option of adding a reversing cylinder to the mix and then another printing unit for each color. So, eight in total for four colors.

Therein lies the main disadvantage of offset printing: It may be fast (120,000 pages per hour), result in high-quality prints, and be ideal for long print runs. It’s expensive and incredibly technical though, generally requiring special operating expertise.

Screen Printing Method

The screen printing process, as its name would suggest, involves ink being forced through fabric (or screen) onto the image areas of the printing surface. Also known as porous printing for obvious reasons, it culminates in a squeegee pushing the ink through, while a stencil, manually cut or made electronically, prevents the non-image areas from getting colored. The process is repeated for each color on a new screen.

The benefits are such that the process can be used on a wide range of substrates, which don’t have to be flat for an effective job to be done. T-shirts are one example of a product printed using this method. Electronic circuits are another. Screen-printing equipment can be relatively inexpensive and the process itself is simple and suitable for small-scale jobs

Digital Printing Method

Two types of digital printing make up the lion’s share of the jobs in this space: Inkjet and xerography. Inkjet printers effectively spray the ink on the substrate in tiny dots that appear as solid colors from afar. Xerographic or laser printers rely on a charged internal cylinder to attract toner that gets transferred to the substrate. While you might use a laser printer for everyday office work, large-scale print shops use them as well for a variety of print jobs.

Digital printing’s lack of contact between the master and substrate makes for great versatility, enabling a wide variety of materials, both delicate and not, to be used as printing surfaces. Digital printing is great for short (and, more and more, long) runs, even allowing for variability between individual prints. Some examples include mailing addresses and, much more famously, The Coca-Cola Company’s campaign featuring personalized names on bottles. Each print can be completely unique, offering a degree of flexibility that other methods can’t.

As digital printing is more so the product and subsequent focus of technological advancement, it stands to gain more ground in the industry. In 2017, digital printing accounted for 16.2% of the global print market. While lithography still dominates (70%), digital is up from 2.9% in 2012, indicating potential for exponential growth moving forward.

Nevertheless, regardless of the technology at your disposal or your preferred printing method, digital tools that promote error-free quality control are readily available. Check for content errors during the pre-press phase and verify samples early on, in the middle, and at the very end of the actual job.

Prevent wasted resources in case of print defects and ensure the print quality stays high throughout. Contact GlobalVision for more details on how to incorporate a custom solution tailored to your specific printing situation into your workflow.

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GlobalVision Desktop 5.4

Date: February, 2019 | CategoryCompany Author: Ryan Szporer


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&lt;p>Many within the quality-control community should be excited about the latest GlobalVision 5.4 release for desktop. None more so than system administrators, whose lives get a lot easier with a brand new access level to assign to users.<!–more–></p>

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<h3 id=”h-top-new-features-include”><strong>Top new features include:</strong></h3>
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<ul><li>The “Approver” access level, which lets standard users review inspection reports.</li><li>The ability to rename access levels to fit corporate preferences.</li></ul>
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<h2 id=”h-approvers-join-the-ranks-of-admins-managers-users”><strong>Approvers Join the Ranks of Admins, Managers, Users</strong></h2>
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<p>Up until now, GlobalVision system admins could assign new users one of three access levels:</p>
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<ul><li>Administrators like them.</li><li>Managers.</li><li>Standard Users.</li></ul>
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<p>The status quo now changes with the addition of “Approvers” to the system.</p>
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<div class=”wp-block-image”><figure class=”aligncenter size-large”><img src=”https://blog.globalvision.co/wp-content/uploads/2020/03/gv-5-4_image1.png” alt=”Screenshot of user editor in GV tools” class=”wp-image-1256″ title=”gv-5-4_image1″/></figure></div>
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<p><br>In addition to being able to exclusively create and edit user profiles (and assign them access levels), Administrators share the same privileges as Managers. Among other abilities, they&nbsp;<a href=”https://blog.globalvision.co/quality/the-importance-of-an-audit-trail-to-securing-data-integrity/”>can view the application’s Audit Trail</a>&nbsp;and customize workflows and inspection profiles. Standard Users can only run and review inspections and generate reports.</p>
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<p>By default, Approvers fall somewhere in the middle in terms of the scope of their privileges. In addition to being able to run inspections (and generate reports), they can also view the Audit Trail, but only to access, review and, of course, approve previous reports.</p>
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<div class=”wp-block-image”><figure class=”aligncenter size-large”><img src=”https://blog.globalvision.co/wp-content/uploads/2020/03/gv-5-4_image2.png” alt=”GlobalVision Audit Event Description and Signature Screenshot” class=”wp-image-1257″ title=”gv-5-4_image2″/></figure></div>
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<h2 id=”h-globalvision-makes-a-name-for-itself-and-its-access-levels”><strong>GlobalVision Makes a Name for Itself and Its Access Levels</strong></h2>
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<p>Admins also reserve the option to rename both the Approver and Manager access levels. This feature comes in handy to clarify roles and responsibilities within your company. Combined with their ability to adjust the minimum access levels to both approve reports and view the Audit Trail, Administrators are able to fully customize the user experience to suit their and their firm’s needs.</p>
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<div class=”wp-block-image”><figure class=”aligncenter size-large”><img src=”https://blog.globalvision.co/wp-content/uploads/2020/03/gv-5-4_image3.png” alt=”GlobalVision Electronic Signature Feature Screenshot” class=”wp-image-1258″ title=”gv-5-4_image3″/></figure></div>
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<h3 id=”h-other-updates”><strong>Other Updates:</strong></h3>
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<ul><li>Optional custom-color highlights on detected differences.</li><li>A new keyboard shortcut to show/ hide difference boxes and identification numbers.</li><li>The ability to enable/ disable email notifications to users.</li></ul>
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<p>As of the GlobalVision 5.4 release, email notifications containing critical information like temporary passwords can be sent to individual users upon the creation of their accounts, for one example. To benefit, administrators just need to set up their own easy-to-configure SMTP (Simple Mail Transfer Protocol) in the application. Administrators can alternatively opt for on-screen pop-up messages containing the same info. The option gives them further control over how they use GlobalVision 5.4 and the degree to which they take advantage of the application’s in-depth feature set.</p>
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Many within the quality-control community should be excited about the latest GlobalVision 5.4 release for desktop. None more so than system administrators, whose lives get a lot easier with a brand-new access level to assign to users. Read more

5 Ways to Make Your Packaging Child-Resistant

Date: February, 2019 | CategoryProofreading Author: Mike Malz


 

There are several reasons why parents tend to keep their medicine stored away in a cabinet that’s too high for their children to reach.

The main reason is simple: Some pills are dangerous for children to ingest and can cause serious harm. Child-resistant packaging, also referred to as “special packaging,” is used to reduce the risk of poisoning in children under the age of five due to how it is significantly more difficult for them to open.

Products such as over-the-counter medicine, pesticides, and household chemicals are potentially hazardous to children. According to the Poison Prevention Packaging Act (PPPA), this does not mean that all packaging or its contents are harmful. This is simply a way for companies to take precautionary measures. Aspirin, some ibuprofen, and mouthwash products are just some that are approved to be child-resistant. But how can businesses apply these child-resistant protocols?

We bring you five ways how to make your packaging child-resistant.

How to Make Your Packaging Child-Resistant 

  • Dexterity: Usually, young children develop their motor skills around eight years old. However, at a younger age, they can push and turn containers and open them, but not simultaneously. The applied force needs to be added to the packaging by a user. Toddlers do not have the strength required to force their way into a package. If companies designed their packaging this way, it would make it more difficult for a child to succeed in opening a container.

  • Avoid visual cues: Many businesses include visual aids such as shapes and colors to instruct the user on how to open the package. Children are naturally drawn to shapes and bright colors. This can be problematic because, given enough time, they will be able to open the packaging. According to Healthcare Packaging, using visual cues that are unique to adulthood will be unappealing and unrecognizable to toddlers. Using text instructions on labels would also be a better option.

  • Increasing the packaging size: Making packaging larger is a simple way to make something child-resistant. For instance, if a user needs two fingers to open a container, it should be customized to fit the fingers of an adult. This method, in combination with applied force, would, in turn, make it harder for a child to open the package. The smaller the size of the container, the easier it becomes for young hands to get into it.

  • Put your packaging to the test: To stay compliant, it’s important to test the packaging and its closure. This is done by performing a routine test with children who are put into groups. Fifty children, usually no more than five years old, are separated into three categories per test. The toddlers are instructed to open the containers with their teeth in a 10-minute time frame. For safety purposes, no more than 200 children can be tested at one time.

  • Unit-dose packaging: It’s common for most pharmaceutical companies to package their pills in bottles. The small containers have caps that can easily be twisted off, giving children the opportunity to open the bottle freely. Some companies, such as McKesson, have developed packaging that is in a single-dose format. The pills come out with a thumb press to release the medicine from its unit. However, the force needs to be applied to the package, something children do not have as previously discussed.

Testing & Certification Process for Child-Resistant Packaging

One way businesses can test their products is through the Consumer Product Safety Commission (CPSC).

They are a United States government agency that works to “reduce the risk of injuries and deaths from consumer goods products by developing voluntary standards within the industry.” Companies can receive a Certificate of Conformity by sending their products in to be tested. Although the testing process is not publicly available, the types of goods are on their website.

Another valid certification for child-resistant packaging is by complying with the ISO 8317:2015 standard.

The International Organization for Standardization defines this standard as specifying “performance requirements and test methods for reclosable packages designated as resistant to opening by children.” In addition, this method was created to not only provide guidelines to restrict children from accessing packaging, but to also allow adults to easily open packaging.

In other words, it’s a double-edged sword. The ISO 8317:2015 child-resistant packaging standard is updated every few years and the public is notified. However, if anyone wants to see the requirements and the testing procedure, they must purchase the PDF version.

Child-Resistant: Safe Products, Safer Packaging

There are so many elements industry leaders need to consider when developing and designing their packaging. In addition to the most common factors, like a clean design and brand awareness, businesses must also include safety elements.

If companies are concerned about whether their packaging is child-resistant, it would be best to comply with the CPSC or ISO 8317:2015 standard. Having either of these certifications will show that they are taking the necessary precautions to ensure their customers’ health and safety.

Companies need to understand some of their customers are parents and have their own set of worries. These clients want to know the products they’re bringing home are child-resistant. What consumers must also remember is that this “special packaging” should be a last resort when it comes to safety.

Medicines that have the potential to harm children should still be kept out of reach. It is recommended that they are left in medicine cabinets or anywhere higher up and out of sight. Products like medicine and consumer goods are meant to promote the well-being of the public. Businesses need to ensure their packaging is just as safe as the products they are offering.

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Ensure your content is always error-free in record time with GlobalVision. Try it now for free. 

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