Validation of biorelevant in vitro dissolution testing method for lamotrigine in formulated dosage form

By:

ANUSHA CH

Material type: Film

FilmSubject(s):

Quality Assurance in Pharmceuticals

DDC classification:

615.190 068 5

Dissertation note: Dissertation 1905-07-04

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Holdings
Item type	Current library	Home library	Collection	Call number	Status	Date due	Barcode
ACP-Thesis & Dissertations	Acharya & BM Reddy College of Pharmacy	Acharya & BM Reddy College of Pharmacy	Quality as	615.190 068 5 (Browse shelf(Opens below))	Available		ACP-T186

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Previous	615.190 068 5 RP-HPLC-method development validation of zinc for the estimation of ornidazole in rabbit plasma and colon	615.190 068 5 Bioanalytical method development and validation of olmesortan medoxomil and metroprolol succinate combination drugs in rabbit plasma by RP-HPLC method	615.190 068 5 Method development and validation for estimation of lamotrigine in marketed formulation	615.190 068 5 Validation of biorelevant in vitro dissolution testing method for lamotrigine in formulated dosage form	615.190 068 5 Development and validation of new analytical technique for the estimation of aceclofenac paracetamol and rabepreazole in pharmaceutical dosage form	615.190 068 5 Method development and validation for simultaneous estimation of glucosamine and ibuprofen in pharmaceutical dosage form by analytical method	615.190 068 5 COO Quality Control in the Pharmaceutical Industry Vol.1	Next

biorelevant ; development ; dissolution ; dosage ; estimation ; for ; form ; formulated ; formulation ; lamotrigine ; marketed ; Method ; testing ; validation ; vitro

Dissertation 1905-07-04

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