Section 5 Slides rev 3.1 CSMO
Section 5:
White Paper Template
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 1
The White Paper Template
, Use the white paper template for the forum the change will be presented at
o Templates are available on that CCB’s web page
, The PCCB uses different WP templates
, Materials uses a "combined" white paper template (CSMO/ATMO) which will be
discussed in this class
In this section, we will examine the white paper template and discuss how to complete it. Occasionally additional foils are presented during the template instruction to further explain specific portions of the template. These pages are indicated with the heading “White Paper Notes” at the top of the page. Pages without this heading are directly from the white paper template.
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 2
MCCB White Paper
Horizon Schedule #: Assigned by MHS web tool ()
Title of the Change: Brief description of the change.
PWP Date: Revision: 0 Will this PWP generate multiple FWPs?
Yes No
FWP Date: Revision: 0
Update revision number each time a submission is made to the CCB. It is your choice whether or not you prefer
to revise the submittal date.
Supplier Change Classification: MCCB: Class A Class B Class C Class C-N
Refer to Spec 08-2091 for definition of Change Classifications
Intel PCCB (if applicable): Class I Class II Class III Class III-N Class IV
PCCB Horizon Schedule #:
Classification Justification: Provide information on potential impact, risk assessment or other data available to justify change classification.
Commodity: List all commodities affected
Supplier: List all Suppliers affected
Intel Sites Affected:
List the VF sites that are affected by the change or run product affected by the change
Divisions Affected:
List the Intel Divisions affected by the change.
Products Affected:
List the Intel Products affected, Platform, part numbers, etc.
Name of Originator: Put name of person who originated this paper and an Intel change owner name if a supplier originated it
Reason for Change: (Brief)
Some examples are: Capacity Increase, Productivity Increase, Quality Improvement, Yield Improvement, Cost
Reduction, EHS, etc.
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 3
Change Description:
Explain what is changing, describe before/after differences, consider all aspects of possible change: tooling, equipment make/model, chemistry, location, etc.
Enter Change Description diagrams, sketches, or flowcharts here. Delete this page if not needed. Add in tables, diagrams, etc to document and illustrate the change
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 4
Change Team:
The first column, “X if req?d” will indicate those functions that are on the change team. The X?s already there
indicate the standard set that should appear on every change team. Additional members will be added depending
on the change. The “PWP Approval” column will be used to indicate when that person has given PWP approval.
The “FWP Approval” column will be used to indicate when that person has given FWP approval.
X if Area PWP FWP Name
req’d. Approval Approval
Intel Sponsor
Supplier Sponsor
QRE
Statistics
JQT List Members Below by Site
CR
CV
IR
KM
CAT/ATD
CSMO
ATD/MTD
AMCL
Design
Finance
Integration
VF Module/JET
Other
ECO /ECR Classification*: BOM Change New part number
*A change checked here requires Configuration Management on the Change Team
Proposed Implementation Date: WW
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 5
Risk Assessment: Low Medium High
Consider all aspects of the change such as availability, technology risk, quality, reliability, customer risk, etc.
associated with implementing the change or not implementing the change. Refer to “Materials Risk Assessment” (Spec.# BS-CSG-0004) for a description of each risk level.
Explanation of Risk Assessment:
Whether you check Low, Medium or High above, explain why it is that level of risk.
Implementation/Synergy: This table should contain only those who are responsible for implementation of the
change and/or ensuring synergy across multiple factories (Intel and/or supplier). This is *not* the change team.
“PWP Synergy” and “FWP Synergy” columns should be used to indicate that person is aware of and agreed to
that ownership.
Site Sponsor PWP FWP Brief Description of Support
Synergy Synergy
THESE TWO TABLES SHOULD BE USED ONLY FOR AR?S ASSIGNED BY THE MCCB. THEY SHOULD NOT BE USED TO TRACK AN AR FOR SOMEONE PRIOR TO SUBMISSION OF THE PAPER.
PWP Actions required by MCCB Owner Due Completed
WW
WW
WW
WW
FWP Actions required by MCCB Owner Due Completed
WW
WW
WW
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 6
Use the Concerns/Consideration sections below to identify and discuss any additional details about the change and
the qualification strategy. For example, explain:
, business implications of implementing versus not implementing
relationship of this change to other changes ,
, rationale for selection of quality characteristics
, logic of qualification plan
, critical logistical considerations or hinge factors
, physical mechanism and models
Supplier Concerns/Considerations:
Intel Concerns/Considerations:
Customer Concerns/Considerations:
Other Concerns/Considerations:
Inventory Control:
Note: Revenue product refers to Intel?s shipments to its customers.
Check the appropriate box in the PWP column based on what you plan to do at time of PWP submission. Then,
when the FWP is submitted, use the FWP column to indicate what actually happened. Only one box should be
checked in each column.
PWP FWP
Revenue product will not be (was not) used.
Revenue product will be (was) used, but will be (was) held until FWP approval.
Revenue product will be (was) used and shipped prior to FWP approval.
Provide explanation if different:
Explain reason for changing strategy and decision process used to support it.
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 7
GANTT CHART
(Complete for PWP and update as necessary for FWP)
KEY: C = Complete; I = In Progress; N = Not Done; NA = Not Applicable
WW WW WW WW WW WW WW WW JET FWP Approval MCCB FWP Approval Spec Update Training Guides Training Implement @ Supplier
Site/Prod.
state site/
location
Site/Prod.
Site/Prod.
Site/Prod.
Implement @ Intel
Site/Prod.
state site/
location
Site/Prod.
Site/Prod.
Site/Prod.
Site/Prod.
Site/Prod.
Other
DCCB Buy-off RFC ECO Approved ECO Effectivity
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 8
White Paper – Notes
Change Proliferations:
In cases where it is not possible to simultaneously implement a change at all sites:
, The proliferation plan must be clearly defined in the PWP. This
plan must comprehend equipment and material handling requirements.
PWP Modifications:
Any significant change to an approved PWP requires re-approval by the Supplier and
Intel CCB. This includes:
, Change in scope
, Change in sites affected
, Change in the Experimental Strategy
Data Sharing
, Data from other sources may be used to justify the change
o Technical Reports
o Other White Papers
o Other products or platforms
, Applicability of the data must be justified
, Shared data used in the qualification should be described and documented in the
White Paper
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 9
KEY INDICATOR SUMMARY
(Complete for PWP and update as necessary for FWP)
No Change – Decrease -- Increase
INDICATOR: SUPPLIER INTEL IMPACT
IMPACT
Process Capability No Change No Change
Yield No Change No Change
Output Quality No Change No Change
Reliability No Change No Change
Productivity No Change No Change
Capacity No Change No Change
Cost No Change No Change
Safety/Ergonomics No Change No Change
Return on Investment No Change No Change
Availability No Change No Change
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 10
COMPLETE TABLES A THROUGH D FOR PWP
DO NOT CHANGE FOR FWP
TABLE A
PROCESS FACTORS
Process Factor Present Value Proposed Value
List out all aspects of the process related to the scope of the change, whether they change or not.
Process factor:
, Parameters whose values are changing
, Process factor values completely describe the change
, Present value describes current condition
, Proposed value describes new condition
, Examples: procedures, equipment, parameter settings, materials, hardware, software, metrology, lot size, etc.
Note: Always indicate the unit of measure for the data indicated.
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 11
COMPLETE TABLES A THROUGH D FOR PWP
DO NOT CHANGE FOR FWP
TABLE B
QUALITY CHARACTERISTICS
Quality Measurement Ideal Present Present Expected
Characteristic Method Target Mean Std Dev Change
Quality characteristic:
, Output response
, Any measure of the product or process that may be affected by the change , May include: module (process) key manufacturing responses, line yield, product quality, product reliability,
manufacturing /operations responses, etc.
, Examples:
, reliability test performance (HAST, temp cycle)
, yield (mechanical, electrical, visual)
, defect level (voids, blisters)
, DPM (visual inspection, electrical outgoing)
, key process parameter (coplanarity, wire pull, thickness)
Measurement method:
, System used to quantify the change in or performance of the quality characteristic , Provide clarification on defect categories or failure rate of concern , Define „failure? for pass/fail type data
, Be specific in the type of data to be gathered and compared
Ideal target:
, Value of the quality characteristic at its highest level of quality , May not be achievable but reflects the most desirable direction for that quality characteristic to move
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 12
Present mean and standard deviation:
, Most recent measures of quality characteristic at current process factor setting. If data is not available,
experimental strategy might call to collect it. In this case, present values should be TBD.
Expected change:
, Indicate direction quality characteristic is expected to move
, Always measured relative to current process except when there is no current process data , Possible Options: No change (no expected change in the characteristic), Better (characteristic moves toward
the ideal target), or Worse (characteristic moves away from the ideal target).
Note: Always indicate the unit of measure for the data indicated.
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 13
COMPLETE TABLES A THROUGH D FOR PWP
DO NOT CHANGE FOR FWP
TABLE C
NOISE FACTORS
Noise Factor Range of Values /Scope Range Evaluated
Noise factor:
, Process or environment variable that naturally changes during manufacturing operation , May influence the measured value of the quality characteristic
, Controlled or uncontrolled: controlled factor is one whose value may be assigned at any time to any level (e.g.
material lot), and uncontrolled factor is one whose value is random & may assume any level in the
manufacturing environment (e.g. humidity)
, A quality characteristic at one module can be a noise factor at a downstream module.
Range of values /scope:
, Entire set of noise factor values over which the change must perform
o For discrete, controlled factors; list the number of values available
o For continuous, uncontrolled factors; list the consumption (or replacement) rate OR size
Range evaluated:
, Subset of noise factor range to be evaluated in experiment
, Full range of noise factor is not always evaluated in an experiment strategy , Justify elimination of significant noise factors in Other Concerns /Considerations section of PWP. , Examples:
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 14
o Number of machines
o Environmental control (temperature, humidity)
o Product type
o Raw material batch
o Shifts, technicians
o Tools, fixtures, manufacturing lots
o Number of VF manufacturing lines
Note: Always indicate the unit of measure for the data indicated.
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White Paper – Notes
Experimental Strategy - Qualification Plan
Objective of Experimental Strategy:
, Define Quality Characteristic performance for the proposed change in
Process Factors across all Noise Factors
, Demonstrate statistical equivalence or better
INPUTS OUTPUTS PROCESS
Quality Process
Characteristics Factors
Table A: Table B: Describe the Measures of Change Process/Product Noise Table C: Performance Factors Range of
Application of the
Change
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 16
White Paper – Notes
Purposes of Tables A, B, C and D in the White Paper
1. Use as a tool to develop the qualification plan.
2. Present all variables in a standardized format that can be clearly
understood and discussed.
3. Identify all the applicable variables:
, Process Factors (Table A)
, Quality Characteristics (Table B)
, Noise Factors (Table C)
4. Identify which variables will be evaluated.
5. Document how the variables are measured.
6. Identify potential interactions between variables.
7. Describe the experimental design (Table D).
8. Define the sampling plan and sample sizes.
9. Define the acceptance criteria.
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White Paper – Notes Table A – Process Factors Example:
Process Factor Present Value Proposed Value Cure Time 60 minutes 15 minutes
Acid Concentration 10% 20%
Substrate Length 5.0 inches 4.8 inches
Alignment Mark Design Cross Circular
Mold 4 cavity 8 cavity
Resin Supplier AAA Resin Company Top Resin Company
Manufacturing Location Columbia, Missouri San Diego, California
Change Control for Materials MTL008986 Rev 3.1 (CSMO) May 2002 18
White Paper – Notes
Table B – Quality Characteristics Example:
Quality Measurement Ideal Present Present Expected
Characteristic Method Target Mean Std Dev Change
Electrical Shorts HP Tester 0% 3.5% NA Improve Solder Thickness Cross Section 1 micron 10.0 2.0 Decrease
microns microns mean Outgoing mechanical Visual Inspection 0 dpm 50 dpm NA None defects
Viscosity Viscometer 10000 kcps 10500 800 kcps None
kcps
Heat Slug Fillet Voids X-Ray 0/part 5/part NA Improve
EXERCISE 4
Please refer to Exercise 4 in the Student Handout.
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White Paper – Notes
Table C – Noise Factors Example:
Noise Factor Range of Values/Scope Range Evaluated in
Experimental Strategy
Solder Rosin Lots 3000 units per lot 8 lots
Production lines at ABC 3 lines 2 lines
Heat slug lots 15,000 pcs/lot 2,000 pcs/lot
Shifts at ABC assembly 2 shifts 2 shifts
AAA Solder Company
Solder supplier BBB Solder Inc. BBB Solder Inc.
Operators 6 per shift 2 per shift
Manufacturing line 10 lines #1, #10
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COMPLETE TABLES A THROUGH D FOR PWP
DO NOT CHANGE FOR FWP
TABLE D
EXPERIMENTAL STRATEGY
Exp # Exp Material Quantity Process Factors Noise Factors Quality Accept Criteria
(Table A) (Table C) Characteristics
(Table B)
Summarize experimental plan by listing out each experiment conducted. There may be experiments conducted at the supplier site and/or the Intel site. Details of each experiment will be documented on the following pages. The “Accept Criteria” column is used to indicate if the quality characteristics have to remain the same as current values, or if the point of the proposed change is to shift those values. For example, if the proposed change is to improve yield, then the accept criteria will be a statistically or technically significant increase in yield.
Accept Criteria:
, SE = Statistically Equivalent, based on statistical test of data , SB = Statistically Better, based on statistical test of data , SEB = Statistically Equivalent or Better
, Capable = Cpk > 1.33
, Stable = Process is stable
, TE = Technically equivalent
, GRC = Gross Reality Check. Should only be used when sample sizes are extremely large, or there is a very low risk.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 21
COMPLETE TABLES A THROUGH D FOR PWP
DO NOT CHANGE FOR FWP
TABLE D (continued)
Detailed Description Experiment
Purpose: To document the details of each experiment. To provide sufficient details to
conduct the experiment. Provide details on:
1. Objective of the experiment:
Document what decisions this data will be used to support – Capability, stability, etc.
2. Choice of experimental material and justification:
Indicate test vehicle, live product, part number if change applies to many parts
3. Experiment design:
paired sample retest two sample serial
paired sample split lot one sample
two sample cross-over zero defect sample
two sample concurrent other __________________________
4. Sample size justification for each quality characteristic: Use this table to document the minimum sample size statistically required to detect the stated technically significant delta. If more or less samples will be used, indicate this in the “n actual”
column and briefly explain why.
Quality Characteristic D n n , , ,
Req’d Actual
5. Sample selection
Explain sampling plan to satisfy n required
6. Experiment/material flow
Explain flow for how and where material will be built and tested, insert a flow diagram
on next page if required.
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7. Statistical analysis methods
, N/A if GRC is used.
, One sample t-test/binomial (for one sample)
, Two sample t-test/binomial (for two sample cross-over, two sample concurrent or two sample serial)
, Paired t-test (for paired sample retest)
, ANOVA t-test or k-sample binomial (for more than two groups)
, Capability analysis if Cpk is the accept criteria
, Control charts if stability is the accept criteria
Insert a flow diagram for experimental flow here, if required. Delete this page if not needed.
Use this page to show how material will be built, where samples are pulled, if lots are split, where samples are shipped. This information will also be useful to those responsible for executing the experimental plan.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 23
White Paper – Notes
EXAMPLE: TABLE D
Exp Exp Material Quantity Process Noise Quality Characteristics Accept Criteria # Factors Factors (Table B)
(Table A) (Table C)
1 3 Jones solder 2.25g/lot All # Solder Ionic Content of Solder Paste For
paste lots, 2 Smith Rosin Information
solder paste lots Lots Only 2 3 rosin lots Jones ~6000 All All Solder Flux Residue Defect Level, SEB
solder paste, piece Heat Slug Delamination,
ABC 4331 PPGA parts Chip Capacitor Solder Fillet
Height,
Solder Fillet Defects,
Heat Slug Fillet Voids,
Flux Residue Signature Prior to
Bake,
Flux Residue Signature Post
Bake
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 24
White Paper – Notes
Experimental Strategy Guidelines – Design Efficiency
There are many considerations in selecting an experimental design. A balance must be achieved between statistical
efficiency and practical logistics. Experimental designs are listed below in order of statistical efficiency. Start with
the first and move down until a practical experimental design is identified.
Paired Sample Retest: all units receive both
treatments Paired Sample Retest - Experimental Flow, Works well for metrologies or test condition
changes. Time, Raw data is required from both processes
to perform the analysis.
UnitsRandomize order ofAdvantages application, Removes any unit-to-unit variation from the
comparison. Process 1, Lower sample sizes required for same (POR or New)detectable delta vs. two sample
comparisons.
, No assumptions about current baseline
Process 2needed. (POR or New)
Disadvantages Compare
, Can only be used on process that don’t
permanently alter the experimental units.
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Paired Sample Split Lot: each lot is split at the proposed process factor change such that Paired Sample Split Lot - Experimental Flow? the lot receives the current treatment and the other ? receives the proposed treatment
, Example: each lot is split between two Timeplating baths. Lot, Raw data is required from both processes
to perform the analysis.
Advantages
, Removes any lot-to-lot variation from the
analysis with the assumption that the units
within the lot are essentially identical as far
as responding to the applied treatment Process 1Process 2, Lower sample sizes required for same POR(New)Comparedetectable delta vs. two sample
comparisons.
, No assumptions about current baseline
needed.
LotDisadvantages
, Difficult to administer
, Non-standard process flow.
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Two Sample Cross-Over: both treatments are run concurrently then machines are switched so that all machines eventually run all Two Sample Cross-Over - Experimental Flowtreatments.
, Example: old and new cure profile run on
each of two ovens. LotLotTime, Raw data is required from both processes
to perform the analysis.
Machine #1Machine #2Advantages
, Easier to administer in the factory Process 2Process 1, Can be run as part of the standard process (New)(POR)flow.
, By crossing over, removes any effect from Comparethe machines from the analysis.
, By running concurrently, confounding time Machine #1Machine #2effects are minimized. No assumptions
about current baseline needed. Process 1Process 2
(POR)(New)Disadvantages
, Requires somewhat larger sample size
than the paired tests listed above
Compare, Requires careful sample selection to ensure that results aren’t biased by
differences in experimental material.
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Two Sample Concurrent: both treatments are run concurrently; no swapping. , Example: qualifying a second line. Two Sample Concurrent - Experimental Flow, Raw data is required from both processes
to perform the analysis.
TimeAdvantages
, Easier to administer in the factory
, Can be run as part of the standard process
flow. LotLot, By running concurrently, confounding time
effects are minimized.
, No assumptions about current baseline Machine #1Machine #2needed.
Process 2 Process 1
(New)(POR)Disadvantages
, Requires somewhat larger sample size
than the paired tests listed above
, Requires careful sample selection to Compareensure that results aren’t biased by
differences in experimental material
, Allows for machine-to-machine difference
to possibly confound results by not crossing over.
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Two Sample Serial Pilot: one treatment is run followed by the second treatment.
Two Sample Serial - Experimental Flow , Example: convert machine to a new recipe
or process.
, Raw data is required from both processes
Time Lot to perform the analysis.
Advantages
, Easier to administer in the factory Machine , Can be run as part of the standard process #1 flow. Process , No assumptions about current baseline 1 (POR)
needed.
Compare Disadvantages
, Requires somewhat larger sample size
Machine than the paired tests listed above
#1 , Requires careful sample selection to Process ensure that results aren’t biased by 2 (New) differences in experimental material
, Allows for confounding time effects due to
not running concurrently. Factory
excursions can bias or invalidate results
unbeknownst to the experimenter
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 29
One Sample: the proposed treatment condition is run and the results compared to a fixed baseline value like the design target or the current process mean. , Example: new process is compared to existing CofC data.
One Sample - Experimental Flow, Raw data is only required from the new
process to perform the analysis.
Advantages
, Easy to administer in the factory Time
, Can be run as part of the standard process
flow
, Requires smaller sample sizes than two
sample comparisons.
Disadvantages Lot, Requires careful sample selection to
Compare toensure that results aren’t biased by
differences in experimental material that baseline
receive the treatment vs. the baseline data Machine #1, Allows for machine-to-machine difference
to possibly confound results by not Process
crossing over. (New), Allows for confounding time effects due to
not running concurrently.
, Factory excursions can bias or invalidate
results unbeknownst to the experimenter.
, Baseline data must be substantial, stable,
and well documented.
, Risky approach if the historical baseline
has significant variation or is unstable.
Including relevant sources of noise is
critical.
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Zero Defect Sample: proposed treatment condition is run and no failures are allowed
, A plan which typically requires that the actual yield loss or failure rate be much less than the level we want to demonstrate
, If you expect failures, then do not use zero defects sampling
Advantages
, Requires much lower sample size than one
or two sample binomial comparisons
, Simple analysis, pass on zero defects, fail
on more than zero.
Disadvantages
, Requires that the actual defect level be
substantially lower than the upper
confidence limit.
Experiments should run a control leg (i.e., two sample comparisons) whenever possible.
Only use a one sample test in the following situations:
, It can be shown that the target value from historical data is stable.
, You are matching the first machine/process/material of its kind to a target value. The second instance of this change should
be matched to the current values of the first one, using a two sample comparison. , Zero defect sampling. Zero defect sampling is not suitable for comparing 2 processes.
Statistics training classes contain documentation of Intel’s best known methods for designing and
analyzing data. These BKM’s should be followed whenever possible, and justification provided when a
deviation occurs.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 31
White Paper – Notes
Experimental Strategy Flow
Experimental Strategy Flow Table to Complete
List Process Factors to be Table A
changed.
,
List Quality Characteristics Table B affected by Process Factors.
,
Add Noise Factors, which may Table C
affect the Quality
Characteristics.
,
List the sequence of Table D
experiments that define
the Experimental Strategy.
,
Attach a complete description of Table D
each experiment.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 32
STOP AT THIS POINT WHEN COMPLETING YOUR PRELIMINARY WHITE PAPER
Quality Characteristics Summary
Quality Characteristic Ideal POR POR New New ,
Target Mean Std Dev Mean Std Dev Result (TSD)
or Spec
The first 5 columns in this table will come from information previously documented in the PWP. Add it here and include the new data from the experiments. Results can be indicated as:
, SE = Statistically Equivalent, based on statistical test of data , SB = Statistically Better, based on statistical test of data , SEB = Statistically Equivalent or Better
, TE = Technically equivalent
, Pass or Fail = Passes or fails Gross Reality Check (GRC) criteria. Pass or fail are also used when accept criteria is capability and/or stability , NE = Not Equivalent, data is not SE or TE – provide justification for implementation of change if still planned.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 33
Conclusions:
Summarize key results and implications of the results Recommendations:
Document change team’s recommendations for implementation, rejection, additional data collection, needed follow-up, etc. Include issues/implications, team’s recommendation.
Other Implementation Items / Details/SLI’s:
Document follow-up plans for implementation, what SLI’s or Lot numbers this change will be implemented on.
Results Details: (Attach supporting analyses and graphs here)
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 34
White Paper – Notes
Final White Paper
Purpose:
1. Document the results of the experiments.
2. Provide a conclusion as to whether the change is equivalent, better or worse than the
current process.
3. Provide a recommendation:
, Implement
, Do not implement
, Collect more data
4. Provide historical documentation for future reference.
5. Use as a tool to "sell" customer on needed or proposed
changes.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 35
White Paper – Notes
Final White Paper – Statistical Analysis Guidelines
All experimental data should be plotted and statistically analyzed using the methods documented in the Intel statistical curriculum.
A complete statistical analysis should include:
, Key structure plots, which show the full structure of the raw data.
, Noise factors such as date and machines should be represented in the plots.
, Key plots and tables of summarized data.
, Estimates of differences.
, 95% confidence intervals for differences and effects
preferable to t values and significance levels.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 36
Exercise 5
Please refer to Exercise 5 in the Student Handout.
Change Control for Materials MTL008986 Rev 2.1.2 (CSMO) May 2002 37