To help companies meet recently updated FDA 510(k) requirements, NSF scientists have developed study designs for E&L testing of medical devices.
Audits are central to establishing and maintaining a quality management system. Find out how to get the most out of your audit program.
As regulation increases for high-risk medical devices, manufacturers can take two main actions to strengthen their audit readiness.
As regulators look more closely at drug manufacturing supply chains, secondary reference standards can help assure the quality and purity of excipients.
Find out how leading technology screens supplements for steroids, contaminants and banned substances, including masking and mimicking agents.
Testing Method Selection, Specification Setting & Equipment Qualification
Salt Lake City, UT
GMP Workshop: Warning Letters Galore-Causes and Prevention of Severe Regulatory Action
Effective Quality Systems for Research and Development
PDA FDA Joint Regulatory Conference
AAPS Annual Meeting & Exposition
NSF International Acquires Becker & Associates
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