Method Development, Validation & Transfer  

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Contract Laboratory Services (CLS) > Pharmaceuticals Analysis >> 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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