Week - 1 |
Pharmaceutical Dosage Forms: Classification and Characterization |
Week - 2 |
Pharmaceutical Dosage Forms: Classification and Characterization |
Week - 3 |
The Importance of Quality Assurance and Quality Control |
Week - 4 |
The Identification of active agents and excipients: Qualitative and Quantitative Analyses, Identification of Impurities and Pharmacopeiae Analyses, Importance of Quality Assurance and Quality Control, Aim, Importance, Planning and Application of Analytic Method Development |
Week - 5 |
The Identification of active agents and excipients: Qualitative and Quantitative Analyses, Identification of Impurities and Pharmacopeiae Analyses, Importance of Quality Assurance and Quality Control, Aim, Importance, Planning and Application of Analytic Method Development |
Week - 6 |
Mid-Term Examination Week |
Week - 7 |
Spasifications of the Final Formulations: Morphological Analyses, Particle Size, Zeta Potential, Thermal Analyses, Spectrophotometric Analyses, Chromatographic Analyses |
Week - 8 |
Spasifications of the Final Formulations: Morphological Analyses, Particle Size, Zeta Potential, Thermal Analyses, Spectrophotometric Analyses, Chromatographic Analyses |
Week - 9 |
Spasifications of the Final Formulations: Morphological Analyses, Particle Size, Zeta Potential, Thermal Analyses, Spectrophotometric Analyses, Chromatographic Analyses |
Week - 10 |
Investigation of Bioavailability and Bioequivalency Studies |
Week - 11 |
Investigation of Bioavailability and Bioequivalency Studies |
Week - 12 |
Evaluation of Results of the Analyses and Documentation of Final Report |
Week - 13 |
Evaluation of Results of the Analyses and Documentation of Final Report |
Week - 14 |
Final Evaluation |