Quality by Design approach to simultaneous stability indicating LC-MS method development and validation for four Anti-HIV drugs in APIs and pharmaceutical formulations.

• In: Poster Presentation
• At: Stockholm (Sweden) (2017)
• Type: Poster
• Poster code: P-A-098-Monday
• By: SAHA, Chandni (JSS College of Pharmacy, Quality Assurance, Mysuru, India)
• Co-author(s): Chandni Saha: Quality Assurance, JSS College of Pharmacy, Mysuru, India
  N Vishal Kumar Gupta: Quality Assurance, JSS College of Pharmacy, Mysuru, India
  
• Abstract:

  Backgrounds

  Soaring rise in the number of patients with anti-HIV treatment receiving combination drug regimens and regulatory compliences to science based approaches alarms the need to have fast and robust methods for separation and identification of Anti-HIV drugs. Thus this works focuses on simultaneous stability indicating LC-MS method

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