Abstract

ANALYTICAL METHOD DEVELOPMENT FOR DETERMINATION OF TENOFOVIR DISOPROXIL FUMARATE BY HPLC

Sachin Munde*, Ms. Dhotre Bhagyashree, Ms. Syeda Farheen Fatema, Ms. Shaikh Arshiya, Ms. Naphade Jayshri and Mr. Mirza Nazish Baig

Abstract

Analytical method development and validation play important roles in the discovery, development and manufacture of pharmaceuticals. Method development is the process of proving that an analytical method is acceptable for use to measure the concentration of an active pharmaceuticals ingredient in specific compounded dosage form which allows simplified procedure to be employed to verify that an analytical procedure accurately and consistently will deliver a reliable measurement of an active ingredient in an compounded dosage form.

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