6 articles
Blog · Jun 9, 2026
How to Fix the Document Errors that Drain Capital Projects
In large-scale energy, engineering and construction projects, document errors can cause schedule overruns and contractor disputes. Learn which controls can reduce these risks and how to assess AI-assisted workflows against project requirements.
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Blog · Aug 28, 2025
Your Guide to 21 CFR Part 11 Compliance for Life Sciences with a Modern DMS
21 CFR Part 11 sets the rules for how life sciences companies manage electronic records and signatures, and the stakes couldn’t be higher. From avoiding FDA warning letters to protecting patients and safeguarding brand trust, compliance is essential.
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AI · Mar 4, 2025
AI from Pilot to Product: How to Overcome Obstacles and Generate ROI
Overcoming the year of the “confused copilot” In 2024, many organizations launched Gen AI pilots, particularly those involving “Copilot” technologies for assistants and agents. However, many of these initiatives have yielded underwhelming results.
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Blog · Jun 27, 2023
Adaptation is your key to QMS adoption
When I talk with people about their Quality Management System (QMS), or their plans to invest in one, I’m often asked about who would be best to estimate the risk of change. This is especially important when people are making changes to Quality System Documents.
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Blog · Jun 7, 2023
Empower your legal team with Google collaboration
Everyone can agree that collaboration is important for a business or project to succeed. However, nowadays, globalization is causing corporations to open offices in multiple countries, while remote work continues to increase following the Covid-19 pandemic.
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Blog · May 11, 2023
The shortest path to QMS adoption is though QMS adaptation
Adoption is one of the key aspects of any QMS program. After all, if people resist using it, or are not using it properly, your Quality Management System is likely to fail.
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