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
ASSESSMENT OF HEAVY METAL CONTAMINATION IN PLASTIC MUGS, FREQUENTLY USED AT LOCAL RESTAURANTS OF DIFFERENT DISTRICTS OF U.P. INDIA
A total number of 42 mugs manufactured from plastics (locally made) were purchased and analyzed to determine the level of zinc, nickel, iron and cadmium. All samples were digested with concentrated nitric acid (HNO...
METHOD DEVELOPMENT AND VALIDATION OF SIMULTANEOUS ESTIMATION OF EZETIMIBE AND GLIMEPIRIDE BY RP-HPLC
ABSTRACT A sensitive, selective and precise high performance liquid chromatographic method has been developed and validated for the simultaneous determination of Ezetimibe and Glimepiride in tablet dosage form. T...
DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE SIMULTANEOUS ESTIMATION OF NICOTINAMIDE AND CLINDAMYCINE IN BULK AND PHARMACEUTICAL FORMULATIONS
ABSTRACT The objective of the current study was to develop a simple, accurate, precise and rapid RP-HPLC method and subsequently validate as per ICH guidelines for the determination of Nicotinamide (NIC) and Clinda...
FINGERPRINT ANALYSIS OF HERBAL MEDICINES USING HPLC: AN OVERVIEW
Fingerprint analysis approach using HPLC has become the most potent tools for quality control of herbal medicines because of its simplicity and reliability. It can serve as a tool for identification, authentication and q...
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...