How a Purpose-Built eQMS Improves Compliance in Life Science Organizations
Life science organizations depend on quality management systems (QMS) to improve products, minimize risks, ensure patient safety, and support regulatory compliance.
Life science organizations depend on quality management systems (QMS) to improve products, minimize risks, ensure patient safety, and support regulatory compliance.
I have a bold opinion: The corrective and preventive action (CAPA) process is the second-most important component of your quality management system (QMS). (If you want to know what I think is No.
Credit: IAF CertSearch
As of 2023, more than 27,000 medical device QMS certificates have been issued worldwide, providing confidence in medical devices.
In memory of Al Phadt, Ph.D.
Credit: National Cancer Institute on Unsplash.
On Dec. 9, 2022, the U.S.
The healthcare industry is known for rapidly adopting advanced technologies that offer improved treatment for various diseases.
Photo by John Schnobrich on Unsplash.
In a highly regulated industry like medical technology, manufacturing processes must undergo either process verification or process validation to ensure they’re consistently producing the correct result. The question is, which one should you use?
Having appeared in the early 2000s, connected health technologies have gradually become a game changer in the healthcare industry.
Credit: Marcel Scholte on Unsplash
Nearly a quarter of surveyed healthcare cyberattack victims experienced increased mortality rates following a data br
Listening to customers is critical for healthcare organizations to ensure they’re delivering high-quality care to their patients.
© 2025 Quality Digest. Copyright on content held by Quality Digest or by individual authors. Contact Quality Digest for reprint information.
“Quality Digest" is a trademark owned by Quality Circle Institute Inc.