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User WAYS points
- WAYS Points
- Academic Level
- Corporate Executive
- Working Sector
- Industry / Business
- Highest Degree
- Ph. D.
- Chemistry: Analytical
- Reseach Topic
- Decontamination of Cephalosporin; An environmental hazard
• Shahnawaz Sajid, Najma Sultana and M. Saeed Arayne; "Validation of cleaning of pharmaceutical manufacturing equipment, illustrated by determination of cephradine residues", in Analytical Methods, Royal Society of Chemistry (RSC) 2010, 2, 397 (Top ten accessed analytical method article)
• Shahnawaz Sajid, Syed Shahid Ali, Najma Sultana and M. Saeed Arayne; Preliminary Evaluation: The contamination of levofloxacin on other follow up drug products and cleaning validation of equipment , in South African Journal of Pharmacy 2010(Accepted).
• Shahnawaz Sajid, Syed Shahid Ali, Najma Sultana and M. Saeed Arayne; Cleaning Validation of Residual Ofloxacin on Manufacturing Equipment Surfaces, in PDA journal of Pharmaceutical Science and Technology 2008.
• Shahnawaz Sajid, Syed Shahid Ali, Najma Sultana and M. Saeed Arayne; Validated HPLC–UV method for simultaneous determination of olmesartan, irbesartan, telmisartan and candesartan with combination of hydrochlorothiazide in pharmaceutical formulations and human serum, in Chinese Journal of Chromatography.
• Shahnawaz Sajid, Syed Shahid Ali , S.Fatima Lakha; Review Article Validation and its overview globally, Institute of Biopharmaceutical IBPA, January 2008.
• Shahnawaz Sajid, Guidelines, equipments and supplies for sterile compounding and manufacturing, in askaboutvalidation forum, May 2008.
• Shahnawaz Sajid ,Syed Shahid Ali, Najma Sultana and M. Saeed Arayne. Validated HPLC–UV method for simultaneous determination of pravastatin, rosuvastatin, atorvastatin, lovastatin and simvastatin in pharmaceutical formulations and human serum, Journal of Chemical Society of Pakistan (JCSP) (In Press).
- Research Tags
- Pharmaceuticals, Bio pharmaceuticals, Analytical Techniques, Cross contamination, Validation
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