Laboratory Services (CLS)
> Pharmaceuticals Analysis
Development, Validation & Transfer
ANALYTICAL, BIO-ANALYTICAL, BIO-PHARMACEUTICAL &
CLINICAL METHODS TO MEET STRINGENT REGULATORY FORMS.
uses pre-qualified protocols based on regulatory norms
of ICH, CDER, or CBER. These protocols can also be
customized to meet client requirements.
expert team has developed, validated and transferred
more than 200 methods for clients.
of our methods developed for Residual Solvents have been
accepted for USFDA submissions.
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.
more information on validations, email at