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Data Standardization: How It’s Done & Why…
See how data standardization and subsequent enforcement of data standards enable organizations to…
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What Is an Electronic Health Record (EHR)?
See why physicians and staff agree almost universally that electronic health records save them…
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Pharmacokinetics
Pharmacokinetics plays a vital role in pharmacology for drug formulation; see how the principles…
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What Is PHI?
Individuals share PHI to partake in healthcare services; see how PHI protection is a priority of…
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What Is GMP?
See how GMP guidelines enable consistent product quality, help identify risks associated with…
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Laboratory Information Management Systems (LIMS)
See how Laboratory Information Management Systems (LIMS) streamlines a fundamental lab process…
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A Guide to IQ, OQ, and PQ in FDA-Regulated…
See how OQ, IQ, and PQ provide a proven validation framework that enables the quality and safety…
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EU MDR: European Union Medical Device…
See how the EU MDR harmonizes requirements across the European Union and provides long-term…
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Electronic Data Capture Fundamentals
See how electronic data capture systems improve information management and analysis and…
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21 CFR Part 820
See how 21 CFR Part 820 has the added benefit of embedding GMP that enable safety and optimize…
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CDISC and CDISC Standards
Learn about CDISC, a non-profit organization that develops data standards for clinical data…
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Good Clinical Practice
See how Good Clinical Practice guides studies to ensure that the highest quality data is…
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Electronic Consent: Definition and How It Works
Learn about electronic consent, considered safe and effective in protecting subjects’ rights in…
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GxP
See how understanding, implementing, and maintaining GxP standards is an effective way to provide…
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