Down to The Last Period
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The automated inspection of pharmaceutical packaging has become essential to the day-to-day affairs of companies wishing to attain the efficiency and error-free work that is demanded of them. In addition to the rigorous quality control implemented on the products themselves, it is important to ensure the compliance of packaging and labeling information.
https://blog.globalvision.co/wp-content/uploads/2021/06/images-what-is-gv_topbanner2.png 879 1639 Kayla Caticchio https://blog.globalvision.co/wp-content/uploads/2020/03/gvblog-logo1a-300x65-copy-300x65.png Kayla Caticchio2021-06-21 09:10:032021-06-21 13:52:07What is GlobalVision? How to Instantly Catch Errors with Automated Quality Control Software
For companies in regulated industries, strict labeling and packaging requirements must be adhered to at all times. Failure to comply with these regulations can result in many issues like market delays, complaints, and even recalls. Despite entire quality control departments dedicated to proofreading labels and packaging components, there are many factors that can contribute to letting an error slip by unnoticed. Manual proofreading can be slow, inefficient, and prone to human error, especially when there are multiple product lines and hundreds of SKUs to manage. Automated quality control software, like GlobalVision, helps businesses stop critical errors while eliminating the inefficiencies that come with manual proofreading, so they can get products to market faster without compromising quality.
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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.
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Now more than ever, the demand for safe and effective medical drugs is increasing on a global scale. This means that regulatory affairs teams are working overtime to interpret, apply, and communicate the guidelines received from governing bodies like the FDA and EMA when it comes to developing new drugs.