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The ROI on a Specification Management System: Is It Worth It?

The ROI on Specification Management System: Is it Worth it?

If you’re a packaging or manufacturing professional, you’ve likely experienced the frustration of spending precious time tracking down product/packaging specification data. The manual nature of managing specifications using spreadsheets, shared...

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Tags: specification management, Spec Management, ISO 9001, Compliance

5 Tips for Complying with The FDA's Food Safety Modernization Act (FSMA)

According to recent data from the Centers for Disease Control and Prevention, about 48 million people in the U.S. get sick, 128,000 are hospitalized, and 3,000 die each year from foodborne diseases. The recent changes to the FDA’s Food Safety...

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Tags: FDA compliance software, fda guidelines, food and beverage industry, fsma

How Quality Management Helps You Adhere to ISO 9001 Standards

With consumers placing an increasingly large emphasis on product quality, meeting regulatory standards like ISO 9001 is more important than ever. To keep up with the ISO 9001 group of standards, many companies find a digital quality management...

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Tags: quality management software system, quality management software, ISO 9001, internal audit

Employee Spotlight: Joe Ciriello

Joe Ciriello is DocXellent’s Business Development Manager and resident nature enthusiast. In this development role, he works on sales expansion in the private, public, and government sectors, growing the organization one sale at a time. He also...

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Tags: employee spotlight, DocXellent Employees, document management software company, sales team

7 Steps to Improve Vendor & Supplier Management

No matter how many vendors your company works with, creating an efficient supplier management process and fostering strong relationships with them is essential. When your business success is dependent on third parties to help you deliver your...

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Tags: document management software, save money, supplier collaboration, vendor collaboration, supplier management software

Expert Interview: Best Practices For The Quality Audit Process

We interviewed DocXellent's resident quality audit expert and Chief Technology Officer, Tom Tassias, to learn from his extensive experience with third-party audits and get his insight into how companies can optimize their audit process to improve...

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Tags: document control software, audit, audit readiness, 3rd party audit, quality audit

5 Ways Laboratories Can Simplify ISO/IEC 17025 Compliance

Meeting the ISO/IEC 17025:2017 compliance standards is essential for testing laboratories. Not only does this regulation dictate lab competency, but it also helps demonstrate that your laboratory is performing at par with your internationally...

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Tags: Compliance, laboratory industry, iso 17025, ied 17025

Best Tips For Training Food & Beverage Manufacturing Employees

No matter the size of the company, food and beverage manufacturers should take employee training seriously. Not only does effective training help you create a quality product, but it also helps keep employees safe on the job, increase employee...

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Tags: training management system, Compliance, food and beverage industry, employee training

10 Manufacturing Blog Posts You Might Have Missed

10 Manufacturing Blog Posts You Might Have Missed

Over the past year, our customers have shown interest in blog posts that showed them how to better manage specifications and create efficiency throughout their manufacturing processes. In case you missed them, or just want to take another look,...

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Tags: specification management, manufacturing, industry blog posts, efficiency

5 Ways to Prepare For The New UK Medical Device Regulations

Over the next couple of months, the United Kingdom’s Medicines and Healthcare products Regulatory Agency (MHRA) is expected to roll out new guidance that will alter the way medical device products are regulated. Preparing for this change may be...

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Tags: regulatory, medical device, medical device regulations, UK, UK regulations