When you complete the stability study:

 The system sets the user status COMP (completed) in the stability study. This status
cannot be revoked and it prevents any other user statuses from being set in the
study.
 The system deactivates the testing schedule.

Which of the following documents are considered for procurement documents?

 Quality assurance agreement ( document type Q01)

 Technical delivery terms ( document type Q02)

Which of the following conditions have to be fulfilled for the material to be

immediately posted to unrestricted-use stock? (Required settings are made in the
inspection setup)

 Skip-to-stock

If you assign a task list with inspection characteristics to a production order or

process order after an inspection lot has been created, these inspection
characteristics-

 Are not be taken into consideration in the inspection

What are the various options available to mange test equipment?

 Equipment
 Document master
 Material master

Which of the following restrictions apply if you perform a simplified quality

inspection using the material specification?

 You cannot predefine work centers

 You cannot perform dynamic modifications
 You cannot use inspection methods

Which of the following conditions should be satisfied for an inspection lot to be

created automatically as soon as the warehouse receipt is posted?

 Appropriate inspection type is entered in the material

The following “Quality Certificates” can be created-

 Certificate of Analysis
 Work Test Certificate
 Certificate of Conformity

The Pre-requisite(s) for “Quality Management in Discrete Manufacturing” is/are-

 Execute the Material Requirements Planning

 Run the Cost-Run
While creating a production version for an inspection lot, how the quality will be
affected if the dynamic modification rule specifies that the quality level must be
updated when the usage decision is made?

 the system does not update the quality level now

You have to carry-out “Inspection Planning” in the Automobile Industry space.

What cross-application data will you focus on?

 Batch Classification
 Customer Info record

The stability study process consists of these main phases:

 Initial test, stability planning, stability test

Depending on the valuation parameter used, the sampling plan consists of-

 The sample size and K-factor for variable inspections

 The sample size if “without valuation parameters” was specified
 The sample size, acceptance number, and rejection number for attributive
inspections

You can create sampling schemes:

 Without valuation parameters, if you use the sampling scheme in a sample drawing
procedure or in a sampling procedure that calls for a sample calculation without a
task list
 For variable inspections based on the s-method
 For attributive inspections

The document flow can directly display the following objects:

 Inspection Lot
 Quality Notification
 Sales Order

While maintaining Default settings at plant-level for QM, a user-field definition for
inspection points has to be specified-

 If you do not maintain this field in the task list header, the system copies the
respective settings defined in Customizing into the inspection lot
 By specifying a user field combination in the task list header of each task list, you
can override the plant-dependent settings defined in Customizing

The digital signature enables you to meet the security requirements stipulated in
the Good Manufacturing Practices with regard to the execution of these
transactions. The digital signature ensures that:

 A transaction is only performed by users with special authorization

 The user's name, the signed transaction, the time and date are documented and
cannot be forged

Which is true regarding physical-sample drawing:

  Physical-sample drawing can be subject to a separate confirmation process using a
status scheme.

The Plant Maintenance functions include –

 Managing master data

 Editing maintenance plans and strategies
 Calibrating

The certificate profile controls:

 The selection and order of the characteristics displayed on the certificate

 Lot selection

The quality information record must relate to which of the following, if the
manufacturer part profile defines manufacturer-related QM processing?

 Manufacturer part
 Vendor

Planned orders are scheduled in SNP with just one PDS for a product. How is the
duration and end date of the order derived, if you plan in weekly buckets?

 Control Charts
 Results Recording
 Results History

The inspection point quantities for the last QM-relevant operation are proposed for
the goods receipt posting for the order-

 Only those quantities that are confirmed to PP as yield are taken into account

If a delivery for a product or a material is created, then QM automatically

generates an inspection lot for the inspection relevant delivery items-

 A delivery item is inspection relevant if the corresponding control parameters are

active in the sales processes and in QM
 When a delivery is created, the Quality-relevant settings start to apply

You can manage test equipment as:

 Equipment
 Material

When you create a task list for an inspection lot, which objects are available for
inspection?

 Material
 Equipment

You process the inspection lot in QM that was created by the planning activities
and release of the maintenance order in plant maintenance:

 The items of equipment assigned in the maintenance item are copied into the
inspection lot as objects to be inspected.
Which quality inspection method do you prefer if you want to record results for
several inspection lots?

 Worklist -> Results recording

Which of the following charts take into account only internal process parameters
and not external tolerance specifications?

 Shewhart Chart

Pplicy No.
52250943------24,745
51735271----=12781