1Analysis of Pharmacopoeial compounds in bulk and in their formulations (tablet/capsules/semisolids) by UV Vis spectrophotometer
2Simultaneous estimation of multi-drug component containing formulations by UV spectrophotometry
3Experiments based on HPLC
4Experiments based on Gas Chromatography
5Estimation of riboflavin/ quinine sulphate by fluorimetry
6Estimation of sodium/ potassium by flame photometry or AAS
7Case studies on
• Total Quality Management
• Six Sigma
• Change Management/ Change control. Deviations,
• Out of Specifications (OOS)
• Out of Trend (OOT)
• Corrective & Preventive Actions (CAPA)
• Deviations
8Development of Stability study protocol
9Estimation of process capability
10In process and finished product quality control tests for tablets, capsules, parenterals and semisolid dosage forms.
11Assay of raw materials as per official monographs
12Testing of related and foreign substances in drugs and raw materials
13To carry out preformulation study for tablets, parenterals (2 experiment).
14To study the effect of pH on the solubility of drugs, (1 experiment)
15Quality control tests for Primary and secondary packaging materials
16Accelerated stability studies (1 experiment)
17Improved solubility of drugs using surfactant systems (1 experiment)
18Improved solubility of drugs using co-solvency method (1 experiment)
19Determination of pKa and Log p of drugs.