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NSF – Health Science News

Meeting 510(k) Requirements for E&L in
Medical Devices

To help companies meet recently updated FDA 510(k) requirements, NSF scientists have developed study designs for E&L testing of medical devices.

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Performing Effective, Value-Adding Audits

Audits are central to establishing and maintaining a quality management system. Find out how to get the most out of your audit program.

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PIP & MOM Implants: What You Can Do

As regulation increases for high-risk medical devices, manufacturers can take two main actions to strengthen their audit readiness.

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Using Reference Standards for Excipient Compliance

As regulators look more closely at drug manufacturing supply chains, secondary reference standards can help assure the quality and purity of excipients.

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High-Tech Tools Help Screen Supplements

Find out how leading technology screens supplements for steroids, contaminants and banned substances, including masking and mimicking agents.

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Featured Training

U.S. Dietary Courses

Testing Method Selection, Specification Setting & Equipment Qualification
Salt Lake City, UT
September 18

UK & EU Courses

GMP Workshop: Warning Letters Galore-Causes and Prevention of Severe Regulatory Action
York, UK
September 20

U.S. Pharma Courses

Effective Quality Systems for Research and Development
Cambridge, MA
November 13

More Training

Featured Training

PDA FDA Joint Regulatory Conference
Baltimore, MD
September 10-12

AAPS Annual Meeting & Exposition
Chicago, IL
October 14-18


NSF International Acquires Becker & Associates

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