BioValidity
Overview
Our Process

BioValidity's research process results in information that clearly states the results of peer-reviewed studies-not just one expert's opinion. Over time, we maintain that information, ensuring that new research is accounted for in the context of the entire body of science to date.
  1. First, we assemble the best scientists and experts to form our Research Team and Advisory Board. We look for people with significant experience who are well respected in their fields. Typically, each BioValidity Advisory Board member specializes in one particular area of the knowledgebase, ensuring that we have both breadth and depth of knowledge on the team. We also seek to balance our teams by combining people who have different perspectives on healthcare today, but who are each committed to the philosophy of providing science-backed information.

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  2. After our teams are assembled, the Research Team starts an in-depth search into the appropriate peer-reviewed journals. The databases researched include Medline, CancerLit, IBIDS, Knight-Ridder, American Botanical Council and the German Commission E. The resulting studies are reviewed and sorted.

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  3. At this point, the Research Team identifies the impacts or benefits that have been studied for each substance. These are summarized in a benefit or impact statement, and are written to conform to the FDA's DSHEA structure/function guidelines (see inset to right).

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  4. The Research Team then rates each statement based on the quality and the quantity of the science that supports it. For example, although a statement might be supported by an excellent study, the team would not be likely to give the statement its highest rating if that study was the only one performed to date.

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  5. The Research Team develops supporting information, such as summaries of the source abstracts.

  6. The benefit statements, abstract summaries, and the supporting science are presented to the Advisory Board for their review and approval. If necessary, the Advisory Board edits the statements, ratings, and summaries until they reach agreement.

  7. New research is added to the database as it becomes available, ensuring that all information is current and up-to-date.


FDA Structure / Function Claims
Through the the Dietary Supplement Health and Education Act of 1994 (DSHEA), Congress and the FDA have created guidelines for the kinds of health claims manufacturers can make about the benefits of dietary supplements. DSHEA requires that benefits be described in structure/function claims - statements about the effect of the supplement on a bodily structure or function - rather than as claims about specific diseases. Click here to see more information on the FDA's site.

Click here to learn how BioValidity can apply its unique K*Base knowledgebase development process serve your knowledge management needs through our Consulting Services Division.