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International Journal of Drug Development and Research

  • ISSN: 0975-9344
  • Journal h-index: 49
  • Journal CiteScore: 11.20
  • Journal Impact Factor: 8.24
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days
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Abstract

Optimization technique as a tool for implementing analytical quality by Design

C. MOHAN REDDY*1, RAGHUNANDAN H.VENKATRAM1, HARSHA JINADATARAYA2, C.PAVAN KUMAR1

A process is well understood when all critical sources of variability are identified and explained, variability is managed by the process, and product quality attributes can be accurately and reliably predicted over the design space. Quality by Design (QbD) is a systematic approach to development of products and processes that begins with predefined objectives and emphasizes product and process understanding and process control based on sound science, statistical methods and quality risk management. In an attempt to curb rising development costs and regulatory barriers to innovation and creativity, the FDA and ICH have recently started promoting QbD in the pharmaceutical industry. QbD is partially based on the application of statistical Design of Experiments strategy to the development of both analytical methods and pharmaceutical formulations. The present work describes the development of robust HPLC method for analysis of Eplerenone formulation under QbD approach using Design of Experiments.