D. Pharm Pharmaceutics Exit Exam Syllabus 2024
Chapter 1: Introduction
Chapter 2: Packaging Materials
Chemical Composition, Advantages and Disadvantages of Packaging material like Glass, Plastic, Metal, Rubber.
Chapter 3: Pharmaceutical Aids
Chapter 4: Size Reduction
Chapter 5: Size Separation
- Sieves and standards of sieves.
- Classification of Powder according to Indian Pharmacopoeia.
- Principle, Construction, working and uses of separators.
Chapter 6: Mixing
- Classification
- Principle, Construction, working and application of Double cone blender, Triple roller mill, Turbine mixer, and Silverson mixer homogenizer.
Chapter 7: Filtration
- Theory of filtration
- Type of filters
- Detailed description of Sintered Glass Filter and Membrane Filter
Chapter 8: Drying
Chapter 9: Extraction
Chapter 10: Tablets
- Classification of tablets
- Composition of tablet
- Method of preparation
- Coated and Uncoated Tablets
- Evaluation method of tablets
Chapter 11: Capsules
- Classification of Capsules
- Composition of Capsules
- Method of preparation
- Evaluation method of Capsule
Chapter 12: Liquid Oral Preparations
Definition, Type, Composition, Method of preparation, application, storage conditions and Evaluation methods of the following:
Chapter 13: Topical Preparations
Definition, Type, Composition, Method of preparation, application, storage conditions and Evaluation methods of the following:
Chapter 14: Nasal preparations and Ear preparations
Chapter 15: Powders and Granules
Definition, Type, Composition, Application of the following:
- Dusting Powders
- Effervescent Granules
- Effervescent Powders
- Insufflations
Chapter 16: Sterile formulations
- Eye Drops
- Eye Ointments
- Injectables
Chapter 17: Immunological Products
- Vaccines
- Sera
- Toxoids
- manufacturing methods of Sera, Toxoids and Vaccines
Chapter 18: Quality Control and Quality Assurance
- Definition and Concepts of Quality Assurance and Quality Control
- Current Good Manufacturing Practice (cGMP)
- Concept of Validation and Calibration