Featured Articles
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Improving Quality Through Supplier Audits
6/6/2022
Suppliers and manufacturers working together to improve quality throughout the supply chain creates high quality standards to ensure final products are safe and effective.
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Common Barriers To Adopting A Traditional MES Solution
5/24/2022
We review commonly perceived barriers to adopting a traditional MES solution and how the path to digitization in manufacturing is easier than manufacturers might think.
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How Modern EQMS Solutions Are Powering Pharma’s Digital Revolution
5/13/2022
If your company isn’t at least planning on implementing an EQMS solution or other advanced digital tools, learn why now is the time to start.
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CAPA Overload And Other Perils To Avoid On Your Compliance Journey
4/25/2022
A significant challenge pharma companies that are striving to maintain compliance and get high-quality products to market quickly is corrective action/preventive action (CAPA) overload. Learn how to develop a smarter pharma CAPA management system.
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5 Answers To FDA Computer System Validation Questions
4/8/2022
We answer questions regarding the FDA's indication that a risk-based approach is compliant and significantly reduces the burden on life sciences companies.
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Quality Management Review For Compliance And Improvement
4/6/2022
Read more about quality management review regulations, a typical quality management review and how to ensure the reviews happen on schedule and per procedures.
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FDA Remote “Inspections” During The Pandemic
3/24/2022
Remote inspections can be easy if the company being audited has invested in a quality management system that stores its documents, provides version control, and tracks all changes.
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Clarifying Confusion In Quality Assurance, Control, And Management Systems
3/24/2022
With similar-sounding terminologies, it’s easy to misinterpret their definitions and purposes. Here we demystify the roles of each quality function, ways they differ, and impact on one another.
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How A Robust Manufacturing Software Solution Can Reduce The Frequency And Impact Of Deviations
3/22/2022
Read how to leverage manufacturing software with robust digital tools to increase operational visibility and stay on top of deviations so that they don’t turn into corrective/preventive actions (CAPAs), or worse.
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Medical Device Industry Guide To Selecting QMS Software
3/22/2022
If your company is looking to purchase or develop medical device QMS software, you can’t afford to overlook these 10 most important system capabilities.