This doctoral-level course establishes foundational competency in the science of dietary supplements. Students develop fluency in the federal supplement research systems (ODS, NCCIH, CARDS database, and NIH Reporter) and master comprehensive regulatory science covering DSHEA, the New Dietary Ingredient (NDI) notification process, structure-function claim substantiation standards, and FTC enforcement. Quality science extends to manufacturer-level GMP auditing, interpretation of Certificates of Analysis, ingredient authentication, and adulteration detection. Students build doctoral-level evidence appraisal competency for supplement clinical trials and systematic reviews, apply these skills across major supplement categories, and produce a professional supplement monograph integrating federal evidence, regulatory status, quality evaluation, and safety assessment.
Synthesize and critically evaluate findings from the federal supplement research system (ODS, NCCIH, CARDS database, NIH Reporter, and the ODS Dietary Supplement Label Database), constructing evidence-based practice recommendations that accurately represent the strengths and limitations of federally funded supplement science.
Evaluate and critique the regulatory compliance and risk profile of supplement ingredients, products, and marketing claims using DSHEA provisions, the New Dietary Ingredient (NDI) notification process, structure-function claim substantiation standards, FDA enforcement authority, and FTC truth-in-advertising principles for justifying regulatory judgments appropriate to scope-of-practice boundaries.
Evaluate supplement product quality from both consumer-facing (USP, NSF, ConsumerLab) and manufacturer-level (GMP auditing, batch testing, Certificate of Analysis interpretation, ingredient authentication, and adulteration detection) perspectives, using FDA inspection and safety databases to make professional product recommendations.
Evaluate and justify safety recommendations for dietary supplements by critically synthesizing adverse event data, drug-supplement interactions, contraindications, tolerable upper intake levels, and adulteration risk across major supplement categories and high-risk populations in order to produce defensible clinical safety positions grounded in ODS resources, the Natural Medicines Database, and FDA reporting systems.
Critically appraise the design, methodology, and evidence quality of clinical trials and systematic reviews for dietary supplements, applying the NCCIH evidence hierarchy and GRADE framework to distinguish strong from weak evidence and articulate clinical implications.
Produce a doctoral-level supplement monograph that integrates federal research evidence, regulatory status, quality and sourcing evaluation, safety profile, and practice recommendations in order to demonstrate the capacity to synthesize the full spectrum of foundational supplement science competencies into professional-grade clinical communication.
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Candidates must possess a baccalaureate degree or higher from an institution accredited by an agency recognized by the US Department of Education. Candidates must submit official transcripts directly from the issuing institution along with one professional letter of recommendation. All applicants must be recommended for admission by the ACHS Admissions Committee.
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