Contract
Laboratory Services (CLS)
> Pharmaceuticals Analysis
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Method
Development, Validation & Transfer
CLL
Provides:
FOR
ANALYTICAL, BIO-ANALYTICAL, BIO-PHARMACEUTICAL &
CLINICAL METHODS TO MEET STRINGENT REGULATORY FORMS.
CLL
uses pre-qualified protocols based on regulatory norms
of ICH, CDER, or CBER. These protocols can also be
customized to meet client requirements.
Our
expert team has developed, validated and transferred
more than 200 methods for clients.
Some
of our methods developed for Residual Solvents have been
accepted for USFDA submissions.
Besides
this, we also have an already existing database of
greater than 600 non-compendial methods, which we can
pick from to reduce the development time.
For
more information on validations, email at
validations@choksilab.com .
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