is owned and operated by Marc W. Andersen, Ph.D., RAC. TRIPHASE
has chemists in all therapeutic areas of drug
development including Medicinal, process development,
formulation, analytical, and manufacturing QC. TRIPHASE has over 50 INDs and IMPDs filed in the last 10 years with
no clinical holds.
The U S. Food and Drug
Administration is a scientific, regulatory, and
public health agency that oversees items
accounting for 20 cents of every dollar spent by
consumers. The agency grew from a single
chemist in the U.S. Department of Agriculture
in 1862 to a staff of approximately 15,000
employees and a budget of $4.4 billion in 2014.
Agency scientists evaluate applications for new
human drugs and biologics, complex medical
devices, food and color additives, infant
formulas, and animal drugs.
Beginning as the Division of Chemistry and then
(after July 1901) the Bureau of Chemistry, the
modern era of the FDA dates to 1906 with the
passage of the Federal Food and Drugs Act; this
added regulatory functions to the agency's
scientific mission. In July 1930 the name
was shortened to the present version FDA .
W. Andersen, Ph.D., RAC
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