Pharmaceutics GPAT Mock test/Quiz for 50 Question Mock Test and Quiz: Welcome to Witfire’s specialized Pharmaceutics GPAT Mock Test/Quiz, engineered for those aiming for excellence in the GPAT exam. Comprising 50 incisive questions, this mock test covers the breadth and depth of pharmaceutics, offering targeted practice for GPAT aspirants.
Noteworthy Features:
Focused Question Set
Our 50-question mock test in Pharmaceutics zeroes in on vital topics such as dosage forms, drug delivery systems, and pharmaceutical technology, providing a robust platform for concentrated study and practice.
Intelligent Analytics
Post-completion, access Witfire’s proprietary analytics dashboard to dive deep into the insights of your performance. The dashboard offers a nuanced understanding of your strengths and weaknesses, helping you tailor your future study sessions.
Timely and Relevant
Aligned with current industry practices and research, the 50-question mock test keeps you abreast of the latest trends and updates in the field of Pharmaceutics.
Why Opt for Witfire’s Pharmaceutics GPAT Mock Test/Quiz?
The 50 questions have been crafted to fit snugly into shorter yet effective study sessions, letting you evaluate your readiness in the Pharmaceutics domain for the GPAT exam in an efficient manner.
You Can also Practice Other Quiz also.
Pharmacology Quiz
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Pharmaceutics GPAT Mock test I/Quiz for 50 Question Mock Test and Quiz
Results
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#1. Which of the following mechanisms describes the release of drug from a porous matrix?
#2. The study of how dosage forms interact with the body is termed as:
#3. Which is the most commonly used preservative in ophthalmic preparations?
#4. Which equation is commonly employed for dissolution studies of pharmaceuticals?
#5. Which process involves reduction of particle size in a solid substance?
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#6. What is the chief active ingredient in effervescent tablets?
#7. What is the ideal osmolarity of intravenous solutions relative to blood?
#8. Which polymer is extensively used in the formulation of hydrogel drug delivery systems?
#9. What is the principal rationale behind enteric coating of tablets?
#10. In HPLC, what does the term "mobile phase" refer to?
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#11. Which of the following is a technique for the bottom-up approach in nanoparticle synthesis?
#12. Which type of tablet is designed to float on gastric fluid?
#13. Which drug formulation technique aims to enhance solubility by reducing particle size to the submicron level?
#14. What is the key variable in determining the viscosity of a Newtonian fluid?
#15. Which of the following is a primary packaging material for parenteral formulations?
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#16. What is the mechanism of action of osmotic controlled-release oral delivery systems (OROS)?
#17. Which method is commonly used for sterilization of thermolabile solutions?
#18. Which of the following excipients acts as a glidant in tablet formulations?
#19. What parameter is analyzed in the friability test of tablets?
#20. Which among the following is a common method for enhancing the bioavailability of poorly water-soluble drugs?
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#21. Which isomerism is most critical in the pharmacokinetic properties of drugs?
#22. What is the critical micelle concentration (CMC) primarily dependent upon?
#23. Which technique involves the use of X-rays to measure the particle size distribution?
#24. Which mathematical model is used to describe non-Fickian (anomalous) drug release from polymeric systems?
#25. Which of the following is NOT a parameter in the design space as per Quality by Design (QbD) framework?
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#26. In Quality Risk Management, which of the following methods is a quantitative approach?
#27. What is the critical parameter that dictates the stability of a lyophilized product?
#28. In a SEDDS (Self-Emulsifying Drug Delivery System), what does the term 'Self-Emulsifying' signify?
#29. Which polymorphic form of a drug is usually the most stable?
#30. What is the role of P-glycoprotein in drug absorption?
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#31. Which equation describes the relationship between dissolution rate and solubility in a sparingly soluble drug under sink conditions?
#32. What is the inherent challenge in the formulation of protein-based drugs?
#33. Which of the following parameters is NOT generally considered in the Development and Scale-Up of a freeze-drying process?
#34. In Targeted Drug Delivery, what role does PEGylation play?
#35. What is the principle behind the use of cyclodextrins in drug formulations?
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#36. Which of the following techniques would be most appropriate for particle size reduction to the nanometer range?
#37. What does 'Q3' signify in a Q1/Q2/Q3 sameness test for generic drugs?
#38. Which among the following is a correct method to study 'Polymorphism' in drug substances?
#39. Which Quality by Design (QbD) element refers to the attributes that should be within an appropriate limit, range, or distribution to ensure the desired product quality?
#40. In Nanotechnology-based drug delivery, what is the major advantage of Lipid-Based Nanocarriers?
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#41. What is the mathematical basis for determining shelf-life through accelerated stability testing?
#42. Which of the following methods would be most suitable for the determination of residual solvents in a drug substance?
#43. How does iontophoresis facilitate transdermal drug delivery?
#44. Which mechanism is primarily involved in the release of drug from an osmotically controlled pump?
#45. Which principle is applied in the measurement of particle size through laser diffraction?
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#46. Which is NOT a typical characteristic of a supercritical fluid?
#47. What does the Peppas-Sahlin model describe?
#48. Which of the following surfactants is generally used in parenteral formulations?
#49. In a phase diagram for a pharmaceutical emulsion, what does the Bancroft rule primarily dictate?
#50. What is the main purpose of a 'geriatric' formulation?
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