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Top Five Things Life Science Companies Need to Know about ISO and FDA Requirements

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Life science companies play a major role in the global economy, with revenues expected to reach a staggering $1.5 trillion by 2020.1 Such a rosy forecast is likely to attract innovators and encourage current industry players to blaze new trails.

Inside <em>Quality Digest Live</em> for Sept. 21, 2018

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IMTS was a blast, but it was great to be back home in lovely Northern California this week. On this episode of QDL, we covered the skills that workers need and the innovations that organizations want.

It’s 2018. Do You Know Where Your Medical Records Are?

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Can you imagine a future where the question, “Did you bring a copy of your test results?” becomes entirely unnecessary?

How the Mayo Clinic Built Its Reputation As a Top Hospital

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‘How is it that in the middle of a relatively small town of about 125,000 people in Minnesota, you’ve got the No. 1-rated healthcare system probably in the world?”

FDA Advances Efficient Approaches to Designing and Conducting Cancer Clinical Trials

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During the past decade, advances in understanding of cancer biology have led to the development of targeted treatments that are more effective than the chemotherapies of the past century.

How to Build a Better, Safer, More Welcoming Hospital

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We spend much of our time in buildings, and they can have a profound effect on our well-being, for better or for worse.

The American Chamber of Horrors

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During the early 20th century, Americans were inundated with ineffective and dangerous drugs, as well as adulterated and deceptively packaged foods.

Faster Analysis of Medical Images

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Medical image registration is a common technique that involves overlaying two images, such as magnetic resonance imaging (MRI) scans, to compare and analyze anatomical differences in great detail.

The Bezos-Buffett-Dimon Healthcare Venture

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The new healthcare venture formed by Amazon, Berkshire Hathaway, and JPMorgan Chase announced June 20, 2018, that Harvard

FDA Proposes Process Modernization to Support New Drug Development

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The staff of the U.S. Food and Drug Administration’s (FDA) Center for Drug Evaluation and Research (CDER) always tries to utilize cutting-edge science and up-to-date process management, befitting our stature as the global “gold standard” in drug regulation.

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