Impurities in
Pharmaceuticals
Jordi Labs' inorganic chemists
have specific expertise in elemental
analysis and work with the latest
instrumentation. We provide a quick
turnaround for method development,
validation and analysis.
In early 2018, the Food and Drug Administration (FDA) – with the
support of the International Council for Harmonisation (ICH)
and the U.S. Pharmacopeial Convention (USPC) – established
new guidelines for elemental impurities in brand and generic
drug products. These guidelines, published as USP 232,
concern manufacturers of goods as varied as surgical
bags, filters, tubes, and dietary supplements.
Regulatory pharmaceutical testing for impurities is
subsequently a matter of necessity.
Contact a member of the Jordi Labs team today to learn more.
Integrity,
innovation and
teamwork are the
"Jordi Way".
These core beliefs
have guided our
business since we
started in 1980.
jordilabs.com
Materials Analysis Lab Testing
