CSPT Study Guide 2026

Everything you need to pass the CSPT exam in one place: the exam format, every topic to study, real practice questions with explanations, flashcards, and full-length practice tests. Free, no sign-up needed.

📋 CSPT Exam Format at a Glance

75
Questions
120 min
Time Limit
70%
Passing Score

📚 CSPT Topics to Study (48)

✍️ Sample CSPT Questions & Answers

1. How should corrective and preventive actions (CAPA) be implemented?
Identify root cause, implement corrective action, develop preventive measures, document everything, verify effectiveness

CAPA requires systematic root cause analysis, immediate correction, preventive measures, documentation, and follow-up verification.

2. What USP chapter applies to endotoxin (pyrogen) testing of large-volume parenteral preparations like TPN?

USP Bacterial Endotoxins Test is used to detect pyrogens in large-volume parenterals including TPN formulations.

3. How frequently must viable environmental monitoring (both air and surface) be performed in ISO Class 5 and ISO Class 7 areas of a Category 2 CSP compounding operation per USP ?
Monthly

USP requires that viable environmental monitoring of ISO Class 5 and ISO Class 7 areas in Category 2 operations be conducted at least monthly under dynamic (in-use) conditions.

4. When must environmental monitoring be performed 'at rest' (static conditions) in a cleanroom?
Only during initial ISO classification and after facility renovations

Static (at-rest) testing is primarily used for initial ISO classification and after significant changes such as renovations, HEPA filter changes, or major equipment installation, rather than as part of routine monitoring.

5. Which surface material is most appropriate for cleanroom walls and ceilings?
Smooth, non-porous, and resistant to sanitizing agents

Cleanroom surfaces must be smooth, non-porous, non-shedding, and resistant to damage from cleaning agents.

6. Which document serves as the official, detailed 'recipe' that must be created for a compounded sterile preparation that will be made more than once, ensuring consistency across different batches?
Master Formulation Record

The Master Formulation Record (MFR) is the detailed recipe that provides all necessary information to compound a specific preparation, including ingredients, quantities, procedures, and labeling instructions. A Compounding Record, in contrast, is the log created for each specific time a preparation is made, documenting the lot numbers and personnel involved in that particular instance.

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1. Learn with Flashcards → 2. Drill Practice Tests → 3. Take the Full Exam Simulation
CSPT Study Guide 2026 — Exam Format, Topics & Practice Questions