A REVIEW ON ANALYTICAL METHOD DEVELOPMENT AND VALIDATION

Journal Title: Int J of Pharm Res & Analy - Year 2014, Vol 4, Issue 8

Abstract

Analytical methods development must be validated to provide reliable data for regulatory submissions. Method development is the process of proving that an analytical method is acceptable for use to measure the concentration of an API in a specific compounded dosage form which allow simplified procedures to be employed to verify that an analysis procedure, accurately and consistently will deliver a reliable measurement of an active ingredient in a compounded preparation.These methods are essential for a number of purposes, including testing for quality control release, testing of stability sample, testing of reference materials and to degree of assurance and is an important process in the drug discovery. Although the drug shows good potency, lack of validated analytical method will not allow the drug to enter into the market. This is to ensure the quality and safety of he drug. This review gives ideas about various methods to check the stability of dug and various validation parameters as per various regulatory authorities.

Authors and Affiliations

Bhagyasree T* , Neelam I1 , Ajitha A1 , Uma Maheshwara Rao V

Keywords

Related Articles

CENTRIFUGAL PARTITION CHROMATOGRAPHY: AN OVERVIEW

Centrifugal partition chromatography (CPC) is a new and unique method of liquid-liquid chromatography. CPC enables the separation of components with nearly identical partition ratios, and is performed without the aid of...

 DEVELOPMENT AND VALIDATION OF HPLC METHOD FOR DETERMINATION OF ROXITHROMYCIN FROM HUMAN PLASMA

 A stable, simple, rapid, precise, accurate HPLC method for analysis of Roxithromycin was developed and validated as per ICH guidelines without need of any internal standard. Separation was carried out using X’terra...

METHOD DEVELOPMENT AND VALIDATION OF ATAZANAVIR IN PHARMACEUTICAL FORMULATION BY RP-HPLC METHOD

Present work describes method for determination of Atazanavir in solid dosage form. The estimation was carried out on a Waters ODS (C18) RP Column, 250 mm x 4.6 mm.column with a mixture of Buffer (triethylamine & pH...

 RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS ESTIMATION OF ARTEMETHER AND LUMIFANTRINE IN PURE AND MARKETED FORMULATION

 ABSTRACT A simple, rapid, precise and accurate reversed phase high performance liquid chromatographic method has been developed for the simultaneous determination of Artemether in combination with Lumefantrine. Thi...

DETERMINATION OF REACTIVE OXYGEN SPECIES IN ISOLATED ERYTHROCYTES

Determination of reactive oxygen species (ROS) in erythrocytes have been extensively studied due to its important pathophysiological role in many diseases. Also, studies on the potential of many antioxidants compounds ar...

Download PDF file
  • EP ID EP138315
  • DOI -
  • Views 95
  • Downloads 0

How To Cite

Bhagyasree T*, Neelam I1, Ajitha A1, Uma Maheshwara Rao V (2014). A REVIEW ON ANALYTICAL METHOD DEVELOPMENT AND VALIDATION. Int J of Pharm Res & Analy, 4(8), 444-448. https://europub.co.uk/articles/-A-138315