Quality by Design approach to simultaneous stability indicating LC-MS method development and validation for four Anti-HIV drugs in APIs and pharmaceutical formulations.
- At: 2017 FIP Congress in Stockholm (Sweden)
- Type: Poster
- 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
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.. The access to the whole abstract and the presentation file is available to FIP members and to congress participants of that specific congress.