CPL is a leading
contract development
and manufacturing
organization (CDMO)
providing product
development services
and commercial
manufacturing of
non-sterile liquid
and semi-solid
pharmaceutical
products. Our modern
development,
manufacturing and
testing facilities
are registered and
audited with the FDA
and Health Canada
and have a solid
record of regulatory
compliance. Our
product experience
includes NDA's,
ANDA's, 505b2,
and OTC products,
and we provide
clinical trial
materials through
commercial product
manufacturing. CPL
has completed
substantial
investments in new
filling and
manufacturing
technologies
including new Symex
mixing vessels and
new tube and bottle
filling
capabilities. From
product development
to commercial
production, CPL
provides turnkey
solutions to our
customers all under
one company.
Andrew Kolbert of Avomeen discusses FDA oversight of E&L testing, complications that arise, and the expertise needed to keep up with changing quality standards
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