Question 1) Describe formulations of SVPs with its quality control tests.
Question 2) Explain importance of validation. Describe different phases of process validation with appropriate pharmaceutical examples.
Question 3) Describe the importance of environmental and personal control in parenterals.
Question 4) Write brief notes on:
a) Factorial design method of optimization
b) Total parenteral nutrition
c) Contact lens and lens care products
d) Gowning area in parenterals
e) Parenteral proteins and peptides
Question 5) Describe the concept of oral controlled release dosage forms with its types. Discuss selection criteria and dose calculation of drug for such systems.
Question 6) Explain physicochemical properties of aerosols systems with reference to solution, suspension and emulsion.
Question 7) Enlist methods for preparation of microencapsules. Describe any two methods from coacervation phase separation and any two methods from mechanical encapsulation process in detail. Describe applications of microencapsulation.
Question 8) Write brief notes on:
a) Filling of aerosols in containers
b) Mucosal drug delivery systems
c) Transdermal drug delivery systems
d) Collection, processing and storage of whole human blood
e) Parenteral implants