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SAP C-TS422-2023 Valid Real Test, C-TS422-2023 Verified Answers
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SAP C-TS422-2023 Exam Syllabus Topics:
Topic
Details
Topic 1
- Process Orders in SAP S
- 4HANA: This section covers an introduction to process order components, processing, and relevant master data objects. Overview of Good Manufacturing Practices (GMP) features.
Topic 2
- Managing Clean Core: This section covers the application of clean core principles to enhance business process agility, reduce adaptation efforts, and drive innovation in ERP systems.
Topic 3
- Lean Manufacturing in SAP S
- 4HANA: This section covers repetitive manufacturing master data, line load planning, and Kanban systems.
Topic 4
- Material Requirements Planning in SAP S
- 4HANA: This part of the exam covers an examination of planning strategies, tools, and long-term planning concepts. Overview of MRP fundamentals and lot size procedures.
Topic 5
- Advanced Planning in SAP S
- 4HANA: This section includes an overview of advanced planning fundamentals and master data. Explanation of key tools and processes. Discussion of planning evaluation concepts.
Topic 6
- Introduction to SAP S
- 4HANA Production Planning: This section covers an overview of production planning components, functions, and planning approaches. Exploration of emerging trends.
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SAP S/4HANA Cloud Private Edition - Production Planning and Manufacturing Sample Questions (Q40-Q45):
NEW QUESTION # 40
What are some SAP recommended guiding principles to achieve clean core operations? Note: There are 3 correct answers to this question.
- A. Establish an organizational structure technical foundation transformation methodology for clean core.
- B. Establish regular housekeeping tasks procedures.
- C. Integrate clean core practices in the endtoend value process chain.
- D. Define roles responsibilities as part of a process transformation office.
- E. Establish release management.
Answer: A,D,E
NEW QUESTION # 41
In documentation for MRP in Advanced Planning you read that new orders are created through infinite planning. What does this mean for the capacity requirements of a new order?
- A. MRP assigns the capacity requirements automatically after the last scheduled operation for each work center.
- B. MRP creates the capacity requirements at the earliest possible time.
- C. MRP assigns the capacity requirements automatically to work centers with the earliest available capacity.
- D. MRP creates the capacity requirements without considering existing load on the work centers.
Answer: D
Explanation:
In SAP S/4HANA Advanced Planning (PP/DS - Production Planning and Detailed Scheduling), infinite planning assumes unlimited capacity availability during the initial planning phase. When the documentation states that "new orders are created through infinite planning," it means that MRP generates planned orders without checking the existing capacity load on work centers. Thus,MRP creates the capacity requirements without considering existing load on the work centers(B). This approach prioritizes material availability and scheduling over capacity constraints, leaving capacity leveling to a subsequent step (e.g., using heuristics or manual adjustments in PP/DS).
Option A is incorrect because infinite planning does not sequence capacity requirements after the last operation; it ignores capacity entirely. Option C is not accurate, as "earliest possible time" implies a finite scheduling logic, which contradicts infinite planning. Option D is also incorrect, as infinite planning does not consider available capacity for assignment. This is consistent with SAP's PP/DS documentation, where infinite planning is a preliminary step before finite scheduling.
NEW QUESTION # 42
Which of the following processes lead to an entry in the MRP planning file? Note: There are 2 correct answers to this question.
- A. Changing the storage bin in warehouse management
- B. Changing the procurement type in the product master
- C. Changing the stock in inventory management
- D. Changing the delivery address in transportation management
Answer: B,C
Explanation:
In SAP S/4HANA, the MRP planning file (table MDVM, visible via MD05) tracks changes that trigger MRP to re-evaluate a material's planning situation. Entries are created when:
* Changing the procurement type in the product master(C): The procurement type (material master, MRP
2 view, field: Procurement Type) determines whether a material is produced in-house ("E"), procured externally ("F"), or both ("X"). Changing it (e.g., via MM02) affects how MRP generates planned orders or purchase requisitions, so an entry is added to the planning file (e.g., NETCH or NETPL indicator) to prompt recalculation.
* Changing the stock in inventory management(D): Any stock change (e.g., goods receipt via MIGO, goods issue via MB1A) updates the available stock (MD04). This triggers an MRP planning file entry because it alters the net requirements calculation, requiring MRP (MD01/MD02) to reassess supply versus demand.
Changing the delivery address in transportation management(A) affects logistics execution (e.g., shipment documents), not MRP planning directly-no entry is created.Changing the storage bin in warehouse management(B) (e.g., via LT10) is a WM-level movement that doesn't impact MRP unless stock quantity changes, which falls under (D). This is per SAP's MRP planning file logic.
NEW QUESTION # 43
What will happen in the MRP run if you have created a new MRP-relevant material that supports both in- house production and external procurement?
- A. The MRP run does NOT consider the material; it has to be planned interactively.
- B. The MRP run assumes in-house production.
- C. The MRP run plans the material only if a quotation has been maintained.
- D. The MRP run assumes external procurement.
Answer: B
Explanation:
When a new MRP-relevant material in SAP S/4HANA supports both in-house production and external procurement (procurement type "X" in the MRP 2 view), MRP defaults to a specific behavior unless overridden by additional settings (e.g., source list, quota arrangement). By default,the MRP run assumes in- house production(B). This is because SAP's standard logic prioritizes in-house production (procurement type
"E") over external procurement ("F") when both are possible,unless a valid source of supply (e.g., scheduling agreement, contract) explicitly directs it to external procurement.
Option A is incorrect because external procurement requires a source list or quota arrangement to take precedence. Option C is false, as quotations are not a prerequisite for MRP planning; they are optional for external procurement. Option D is also incorrect-MRP will plan the material automatically based on its master data, not require interactive planning. This behavior is documented in SAP's MRP processing rules.
NEW QUESTION # 44
How can you support a GMP (Good Manufacturing Practice) compliant production process? Note: There are
3 correct answers to this question.
- A. GMP-compliant flag
- B. Recipe approval
- C. Approved resources
- D. Batch record
- E. Digital signature
Answer: B,D,E
Explanation:
In SAP S/4HANA Cloud Private Edition, supporting aGood Manufacturing Practice (GMP)compliant production process (common in industries like pharmaceuticals) involves features to ensure traceability, quality, and regulatory adherence:
* Digital signature(A): SAP supports digital signatures (configured in Customizing, Cross-Application Components > General Application Functions > Digital Signature) for critical process steps (e.g., order release in CO02 or confirmation in CO11N). This ensures authorized personnel approve actions, meeting GMP requirements for accountability andaudit trails.
* Recipe approval(C): In process manufacturing, recipes (process orders use Production Process Models or Master Recipes, transaction C201) require approval (status change, e.g., from "Created" to
"Released" via ECM or C202). This ensures only validated production instructions are used, a key GMP compliance step.
* Batch record(E): The electronic batch record (EBR, transaction COEBR or integrated in process order management) documents all production details (e.g., materials, quantities, quality checks). It's mandatory for GMP to provide a complete, auditable history of each batch (configured via process order settings).
Approved resources(B) isn't a standard SAP term-resources (work centers, CR02) can be quality-checked, but approval is process-driven, not a distinct feature.GMP-compliant flag(D) doesn't exist as a specific field- GMP compliance is achieved through process controls, not a single indicator. This is per SAP's GMP support documentation.
NEW QUESTION # 45
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