Objective. The student will assemble the complete technical report, write a 10 CFR Part 50 Appendix B-based corrective action document for a seeded deficiency in the scenario, and rehearse the oral defense to the point of confident, accurate response to panel questions.
This lesson, its worked examples and its practice questions has not yet been verified by a licensed professional engineer or master tradesperson or by a certification or approval body. It is a study draft and may contain errors. Do not use it as instructions for work on a job site or on live equipment. Always follow your instructor, your supervising professional, and current official references and regulations.
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This lesson marks the culmination of your training program. You will assemble every prior section into one cohesive technical report, write a formal corrective action document rooted in 10 CFR Part 50 Appendix B, and rehearse your oral defense until your responses are confident and accurate. Each task mirrors what nuclear plant staff do every day: document work rigorously, hold each other accountable through the corrective action program (CAP), and defend technical decisions to regulators, supervisors, and peers.
A nuclear technical report is not a collection of separate homework assignments stapled together. It is a single, unified document with consistent numbering, consistent terminology, and a logical flow from front matter to appendices. Use the NEI NUCP Uniform Curriculum document conventions your instructor has provided: consistent heading levels, controlled-document header blocks on each page, revision tracking, and a signature block on the cover page.
Your report must contain six sections in this order:
1. Cover page — plant/scenario name, date, revision number, author, and instructor sign-off block.
2. Table of contents — auto-generated if your word processor supports it; page numbers must be accurate.
3. Executive summary — one page maximum. State the scenario, the major findings, any compliance gaps, and the corrective action disposition. A reader who only reads this page must understand the whole report.
4. Section 2: Regulatory Compliance Matrix — maps each applicable requirement to the specific plant procedure or design feature that satisfies it.
5. Section 3: System Functional Analysis — your reactor systems walkdown and analysis from earlier coursework.
6. Section 4: ALARA/RWP Analog — radiation work permit logic, dose estimates, and ALARA justification.
7. Section 5: LOTO Package — your lockout/tagout isolation steps, energy verification, and restoration sequence.
8. Section 6: Corrective Action Document — described in the next section.
Submit your complete draft to the instructor at least one week before your defense date. This gives time for a formal red-line review. Do not dismiss any red-line comment; every unresolved comment on a safety-critical item — an isolation step, a dose limit citation, or a regulatory reference — will block your report from being cleared as "ready to defend."
10 CFR Part 50 Appendix B, Criterion XVI requires that conditions adverse to quality be promptly identified and corrected. Significant conditions adverse to quality require the cause to be determined and corrective action taken to prevent recurrence. Your Section 6 must comply with this standard.
Your scenario contains one seeded nonconformance — for example, an out-of-calibration instrument, an expired surveillance interval, or a deviation from a procedure step. Work through the following structure, keeping the document to three to five pages:
1. Condition Report (CR) Header — unique CR number (assign one for the exercise), date, system affected, component or procedure identifier, and the author's name and qualification level.
2. Condition Adverse to Quality Statement — one to three sentences that describe exactly what was found, in objective language. Avoid conclusions here; state only the observed fact. Example: "The [instrument tag] calibration sticker expired on [date]; no extension was documented in the surveillance tracking system."
3. Apparent Cause Evaluation Using Five-Whys — ask "Why did this happen?" and answer it; then ask why that answer occurred, and so on, for five iterations or until you reach a root organizational factor. Document each layer. This method is simple but powerful and is widely used in nuclear CAPs.
4. Immediate Corrective Action — the action taken right now to restore the system or procedure to a conforming state. Include who is responsible and the target completion date.
5. Long-Term Preventive Action — the systemic fix that prevents recurrence: a procedure revision, a scheduling system change, additional training, or a design change. Assign a priority level (your scenario CAP description will define the priority tiers) consistent with the significance of the nonconformance.
6. Regulatory Disposition — state whether the condition is potentially reportable under 10 CFR 50.72 or 50.73, or whether it is bounded by existing operability determinations. If you are uncertain, state that an operability determination is required before returning the component to service. In a real plant, this step is never skipped.
The two areas where errors carry the highest consequence in your report are the LOTO isolation package (Section 5) and dose limit compliance (Section 4). A missed isolation point can result in unexpected energy release — electrical, mechanical, hydraulic, or thermal. An incorrect dose estimate can expose a worker to a dose that violates 10 CFR Part 20 limits. The instructor's red-line review focuses here first. Treat every comment on these sections as a safety-critical finding, the same way a plant would treat a CAP item.
The oral defense tests whether you understand your own report — not whether you can read it aloud. Conduct two full mock defenses before the graded event:
Record both sessions if equipment is available. Score yourself on the oral defense rubric your instructor has provided. If you score below 70% on the question bank during the mock session, you must complete an additional coached session before the graded defense date. Use the gap between the mock and the graded event to revisit specific course notes, not to re-read the entire program.
Arrive at your defense with a clean, approved copy of your report and any slides you have chosen to prepare. Speak to your technical content, not to your slides. A panel question overrides any slide you have on screen.
Answer each question, then check it. Nothing is recorded; this is your own practice.
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