Quality Plan
Quality Plan
Quality Plan
ACME Inc.
Document code:
Project:
Prototype
Revision:
Order number:
Date:
PR0001 QP
1.4
16 August 2008
Description
Serial N
PROT
A simple prototype
001/2008
Document approval :
Editor:
Company Name
Responsibility
Name
Supplier
A. Smith
Supplier
R. Green
Customer
Project engineer
M. Brown
Customer
E. Scott
Date
F. Piraneo G.
Signature
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Document PR0001 QP
Table of contents
1. INTRODUCTION........................................................................................................................................................ 2
2. REVISION HISTORY................................................................................................................................................... 3
3. OVERVIEW............................................................................................................................................................. 4
3.1. LINE OVERVIEW.................................................................................................................................................................... 4
4. QUALITY PLAN......................................................................................................................................................... 5
4.1. CUSTOMER QUALITY REQUIREMENTS.......................................................................................................................................... 5
4.2. SUPPLIER QUALITY SYSTEM..................................................................................................................................................... 5
4.2.1. G UIDELINES COMPLIANCE........................................................................................................................................................................5
4.2.2. I NTERNATIONAL AND LOCAL STANDARDS COMPLIANCE......................................................................................................................................5
4.2.3. Q UALITY RESPONSIBILITIES...................................................................................................................................................................... 6
4.2.4. RESPONSIBILITIES................................................................................................................................................................................. 6
5. PROJECT PLAN......................................................................................................................................................... 7
5.1. PROJECT ORGANIZATION......................................................................................................................................................... 7
5.1.1. S UPPLIER PROJECT TEAM........................................................................................................................................................................7
5.1.2. CUSTOMER PROJECT TEAM......................................................................................................................................................................7
6. DOCUMENTATION..................................................................................................................................................... 9
6.1. ACME INC. REFERENCE DOCUMENTATION.................................................................................................................................... 9
6.2. SUPPLIER ISSUED DOCUMENTATION............................................................................................................................................ 9
7. DEVELOPMENT TOOLS............................................................................................................................................. 12
8. PROJECT HANDLING................................................................................................................................................ 13
8.1.1. P ROJECT PHASES............................................................................................................................................................................... 13
8.1.2. I NPUT AND OUTPUT CRITERIA................................................................................................................................................................. 15
8.2. CHANGES......................................................................................................................................................................... 16
8.3. PROJECT MILESTONES......................................................................................................................................................... 16
10. ENCLOSURES...................................................................................................................................................... 22
10.1. SOFTWARE REVISION REQUEST FORM ISSUED BY SUPPLIER....................................................................................................... 22
10.2. SOFTWARE FEATURE REQUEST FORM ISSUED BY SUPPLIER....................................................................................................... 22
ACME Inc. - Good Sunshine Blvd. - Los Angeles, CA USA Phone: +1.123.987.4567 Fax: +1.123.987.4568
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Document PR0001 QP
Version 1.4
1. INTRODUCTION
This Quality Plan/Project Plan has been produced for ACME Inc. by IFACE.
The purpose of the plan is to define the quality requirements of the project, the responsibilities and the procedures applied
by Supplier in order to satisfy the requirements of ACME Inc., CA.
This document conforms to Pharmaceutical Industry GAMP 4 Supplier Guide Procedure for the Production of a Quality and
Project Plan.
The plan covers the activities performed by Supplier for the manufacturing and validation of the following machines:
Item
Machine type
Model
A simple prototype
PROT
001/2008
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Document PR0001 QP
Version 1.4
2. REVISION HISTORY
Revision
Issue date
Description / Changes
Draft A
14 October 2007
1.0
23 January 2008
1.1
07 Supplierch 2008
1.2
06 May 2008
1.3
05 June 2008
1.4
16 August 2008
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Document PR0001 QP
Date 16 August 2008
Version 1.4
3. OVERVIEW
[Suppressed]
The machine will be controlled by an Allen Bradley PLC supported by adequate HMI both interfaced with department wide
SCADA (not supplied by Supplier). Details can be found on hardware design specification documents.
Note the following:
1. [Suppressed];
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Document PR0001 QP
Version 1.4
4. QUALITY PLAN
4.1. CUSTOMER QUALITY REQUIREMENTS
ACME requires that all automated systems, which affect regulatory compliance of their production process, must be
validated.
Supplier will carry out the activities detailed in this plan in order to produce sufficient documented evidence that the system
will consistently meet its predetermined specifications and quality attributes.
The pharmaceutical industry standard life-cycle model for the production of the control system includes the following phases:
Definition of requirements;
Supplier assessment;
specification;
design;
acceptance testing;
procedure definition;
ISPE GAMP-4;
The relevant procedures included in the GAMP-4 guideline are listed below:
Quality and project planning: Appendix M6
Production of a Functional Specification: Appendix D2
Testing of an automated system: Appendix D6
Production of software / module design specification: Appendix D4
Guidelines for document management: Appendix M10
4.2.2. INTERNATIONAL AND LOCAL STANDARDS COMPLIANCE
Manufactured machines will be compliant to the following standards:
Standard
Jurisdiction
73/23/EC
European Directive
Description
Low voltage compliance
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Standard
Jurisdiction
Description
89/336/EC
European Directive
Electromagnetic compatibility
Machinery
98/37/EC
European Directive
21 CFR 211.63
US federal law
21 CFR 211.68
US federal law
NFPA70
US Standard
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Version 1.4
5. PROJECT PLAN
5.1. PROJECT ORGANIZATION
5.1.1. SUPPLIER PROJECT TEAM
The roles of the project team members qualified to the job for Supplier are as follows:
Company
Name
Function
Reference
Person Name
Responsibility
Supplier
General Manager
GM
[Suppressed]
Supplier
Project Manager
PM
[Suppressed]
Supplier
Mechanical Engineer
ME
[Suppressed]
Interface
Supplier
Automation Dept.
Manager
ADM
[Suppressed]
and
electrical
Interface
between
engineers teams;
Supplier
Electrical Engineer
EE
[Suppressed]
mechanical
and
electrical
Automation Engineer
AE
[Suppressed]
Quality Assurance
QA
[Suppressed]
Supplier
Editor
[Suppressed]
Responsibility
Project engineer
Person Name
[Suppressed]
ACME Inc. - Good Sunshine Blvd. - Los Angeles, CA USA Phone: +1.123.987.4567 Fax: +1.123.987.4568
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Document PR0001 QP
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Version 1.4
Responsibility
Person Name
[Suppressed]
Validation engineer
[Suppressed]
[Suppressed]
Project QA
[Suppressed]
ACME Inc.
Process equipment
[Suppressed]
ACME Inc.
QA
[Suppressed]
ACME Inc.
ETS
[Suppressed]
ACME Inc. - Good Sunshine Blvd. - Los Angeles, CA USA Phone: +1.123.987.4567 Fax: +1.123.987.4568
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Document PR0001 QP
Version 1.4
6. DOCUMENTATION
6.1. ACME INC. REFERENCE DOCUMENTATION
Item
Document code
Rev
US1257-T-0B0382
04
[Suppressed]
Description
US1257-T-0A0507
03
[Suppressed]
US1257-T-090508
03
[Suppressed]
US1257-T-060509
03
[Suppressed]
US1257-T-030512
03
[Suppressed]
US1257-T-012345
02
Training policy
US1257-T-001984
01
[Suppressed]
US1257-T-001971
03
[Suppressed]
Deleted
N/A
Deleted
10
US1257-T-001969
03
[Suppressed]
First group;
2.
Second group;
3.
Third group.
Item
Document
Layout drawings and P&ID
including:
Equipment layout in
plan and side views;
Equipment
dimensions and
machine feet layout;
Equipment load;
Consumption (Peak
and mean values);
Cycle times;
Utility connections
type and dimension.
Issues
Support
Electronic
Paper
Approval
Electronic
Paper
Approval
Electronic
Paper
Approval
Electronic
Paper
Approval
Electronic
Paper
Approval
ACME Inc. - Good Sunshine Blvd. - Los Angeles, CA USA Phone: +1.123.987.4567 Fax: +1.123.987.4568
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Document PR0001 QP
Version 1.4
Item
Document
Issues
Support
Electronic
Paper
Approval
Traceability matrix
Electronic
Paper
Review
Electronic
Paper
Review
Electronic
Paper
Review
10
Electronic
Paper
Review
11
Electronic
Paper
Review
12
Electronic
Paper
Approval
13
Software list
Electronic
Paper
Review
14
Instrument list
Electronic
Paper
Review
15
Electronic
Paper
Review
16
Configuration management
Electronic
Paper
Review
17
Electronic
Paper
Review
18
Electronic
Paper
Review
19
Alarm list
Electronic
Paper
Review
20
IQ test protocol
Electronic
Paper
Approval
21
OQ test protocol
Electronic
Paper
Approval
22
HMI manual
Electronic
Paper
Approval
23
Training documentation
Electronic
Paper
Review
24
Hardcopies of application
software & Backup of
application software
Electronic
Paper
25
Electronic
Paper
Review
26
Electronic
Review
Review
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Document PR0001 QP
Document
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Version 1.4
Issues
Support
27
List of components
Electronic
Paper
Review
28
Paper
Review
28
Certificates:
FDA approved
gaskets;
Material certificates
(surfaces in product
contact);
Passivation
certificate;
Filter certificate.
Paper
Review
29
Progress report
Each month
Electronic
Review
30
Electronic
Paper
Review
31
Electronic
Paper
Review
32
Electronic
Paper
Review
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Document PR0001 QP
Version 1.4
7. DEVELOPMENT TOOLS
The items listed below will be used as development tools during this project:
Tool name
Manufacturer or
software house
Release
OpenOffice
Sun
2.4
RSLogix 5000
Allen-Bradley
Actual
RSView Studio
Allen-Bradley
Actual
Performed task
Production of documentation
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8. PROJECT HANDLING
8.1.1. PROJECT PHASES
The project is made in several tasks; diagram has been drawn to underline the activities that can be performed concurrently.
Phase 1
Quality plan / Project plan
issue
Phase 2
Functional design specifications
issue
Phase 3.1
Hardware design specifications
issue
Phase 4.1
Software module design specifications
issue
Phase 3.2
Hardware design
Phase 4.2
Software design specifications
issue
Phase 3.3
Hardware manufacturing
Phase 4.3
Software modules design
Phase 3.4
Hardware post manufacturing testing
Phase 4.4
Software modules bench testing
Phase 4.5
Software integration
Phase 4.6
Software integration bench testing
Phase 4.7
HMI design
Phase 4.8
HMI bench test
Phase 5
Software and hardware integration
Phase 6
Software field test
Phase 7
Internal testing and verification of IQ test
protocol
Phase 8
User's documentation issue
Phase 9
Internal testing and verification of OQ test
protocol
Phase 10
F.A.T. at Supplier's facility
Phase 11
S.A.T. at ACME's facility
Phase 12
S.A.T. and commissioning at ACME facility
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Document PR0001 QP
Name
Redaction, review and approval of FDS (Functional design specifications) for the three
groups of machines:
1. Group 1;
2. Group 2;
3. Group 3.
.1
Redaction, review and approval of HDS (Hardware Design Specifications) for the three
groups of machines as detailed on phase 2.
.2
Hardware design
.3
Hardware manufacturing
.1
Redaction, review and approval of SMDS (Software Modules Design Specifications) for the
three machines as detailed on phase 2.
.2
Redaction, review and approval of SDS (Software Design Specifications) for the three
machines as detailed on phase 2; this document contains the integration specification of
the software modules and design specifications for HMI;
.3
.6
.7
Integration test where bench tested software will be loaded on machine's CPU and HMI;
the functionality of each I/O of each machine will be tested.
Software field test on machines prior to FAT where each functionality of the machines will
be tested.
IQ protocol issue, test on machine, review and approval for the three machines as detailed
on phase 2.
10
11
Manufacturing of the three electrical cabinets and machine's on board wiring as detailed on
wiring schematics issued on phase 3.2.
.5
Redaction of wiring schematics for the three electrical cabinets as detailed in phase 2.
.4
.4
4
Details
Troubleshooting;
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Document PR0001 QP
Name
Version 1.4
Details
S.A.T. and commissioning at ACME SAT and commissioning of the three machine group with the presence of Supplier
facility
engineers; operators and first aid engineers will be trained with training manuals prepared
on phase 8.
Issue
Review
Appr
Procedure
Input
Output
PM
QA
Order confirmation
PM
QA
D1 Production of a functional
specification
User's Requirements
Specifications
Quality Plan
Approved FDS
RTM update
3.1
AE
ADM
PM
D3 Production of hardware
design specification
FDS
Approved HDS
RTM update
3.2
EE
ME
ADM
PM
N.A.
HDS
Electrical schematics
Pneumatical schematics
3.3
EE
ADM
PM
N.A.
Electrical schematics
Pneumatical schematics
3.4
EE
ADM
PM
4.1
AE
ADM
PM
D4 Production of software /
module design specification
FDS
Approved SMDS
4.2
AE
ADM
PM
D4 Production of software /
design specification
FDS / SMDS
Approved SDS
RTM update
4.3
AE
ADM
PM
SMDS
SMDS
SDS
SDS
4.4
AE
ADM
PM
4.5
4.6
AE
AE
ADM
ADM
PM
PM
4.7
4.8
AE
AE
ADM
ADM
PM
PM
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Document PR0001 QP
Issue
Review
Appr
Procedure
Version 1.4
Input
Output
AE
ADM
PM
AE
ADM
PM
ME,
ADM,
PM
QA
D6 Testing of an Automated
System
Approved HDS
ME,
ADM,
PM
QA
Internal procedures to be
referenced
Approved FDS
Approved HDS
Approved SDS
ME,
ADM,
PM
QA
D6 Testing of an Automated
System
Approved SDS
10
AE,
ADM,
PM
PM
GM
D6 Testing of an Automated
System
11
AE
PM
PM
D6 Testing of an Automated
System
D6 Testing of an Automated
System
12
AE
PM
PM
Instrument list;
Historian tag list;
Screen navigation
procedure;
Disaster recovery;
HMI manual;
Training documentation;
Approved OQ
Built version report
FAT approval form
FAT accepted machines
SAT approved form
First SAT accepted
machines
Operator's training
certificates
8.2. CHANGES
For any change on this project involving:
Budget;
Time schedule;
Functionality;
Contract liability;
Notes
Purchase order
Documentation package 1
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Version 1.4
Notes
Documentation package 2
Documentation package 3
FAT
Punch fix and packing
Shipment
Delivery to ACME
Installation in ACME
Alignment
Startup
IQ
OQ and training
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Page 18 of 22
Document PR0001 QP
9.2. PURPOSES
The purposes can be identified as:
Configuration Identification: What code are we working with?
Configuration Control: Controlling the release of a product and its changes;
Status Accounting: Recording and reporting the status of components;
Review: Ensuring completeness and consistency among components;
Build Management: Managing the process and tools used for builds;
Process Management: Ensuring adherence to the organization's development process;
Environment Management: Managing the software and hardware that host our system;
Teamwork: Facilitate team interactions related to the process;
Defect Tracking: making sure every defect has traceability back to the source.
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Document PR0001 QP
Version 1.4
e as experimental version prior to release; indicates a quite stable code where extensive tests are in progress on
machine;
absence of any letter or symbol indicates that the program is stable and released.
<ext> of the file depends on programming environment capabilities and can be a compressed archive like .zip, .rar or .ace or
proprietary file format like .rss or .hmi.
Putting all together:
P00001-1.0-20071110.zip refers as the first version of PLC application program for the machine S/N 00001
released on 10 November 2007;
D00001-w0.5-20071009.ace refers as a pre-release version snapshot on 09 October 2007 of the HMI program of
the above machine.
9.4.2. SOFTWARE MODULE IDENTIFICATION
Identification of software module is quite different from whole program identification due to more limited capabilities in
version indication of many application program IDEs; in such case we can have three release indicators:
<major>.<minor>.<phase>
Major is the major release of the module; as application program, a major release is issued the first time the program leave
the factory or when functionality has been introduced;
Minor is the minor release of the module; a minor release is issued in case of bug fixes or small optimizations; minor
release is always one digit long;
phase can be:
0 - Stable, released;
1 - To be tested on the machine (may be bench tested or not depending if the block can be bench tested);
3 - Edit phase.
When a module is written for the first time, his release will be: 1.0.3; when a module is declared fully working on the machine
and released for the first time, the release will be: 1.0.0.
Version number: 1.1.1 indicates that the block is a bench tested block and has to be tested on the machine; block is based
on 1.0.0 release and has been modified for minor changes like code optimizations.
ACME Inc.;
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9.6. REVIEW
Each module will be tested separately on a test CPU (possibly equal to the CPU is planned to be mounted) against a
module test specification, issued following the requirements of software modules design specifications.
Once the module passed the test it will be integrated following the software design specification document.
At periodical interval, the software engineer responsible for the machine or the automation department manager reviews and
assign all the generated Software revision request form (Enclosure 10.1) for the debug.
When the software engineer acts on the Software revision request form it fills up the action performed and indicates the
status of the request and if the bug has been fixed.
This form will be filled in Italian and will be available for review.
9.7.2. FEATURES THAT HAS TO BE ADDED OR ERASED ON SOFTWARE
When a new feature of the software is needed a Software feature request form (Enclosure 10.2) has to be filled up,
indicating:
At periodical interval, the software engineer responsible for the machine or the automation department manager reviews and
assign all the generated Software feature request form.
This form will be filled in Italian and will be available for review.
2
Starting from project phase 10 and beyond, an incident report will be filled in English and handled as indicated on FAT test plan.
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Date 16 August 2008
Version 1.4
When the software engineer acts on the Software feature request form it evaluates the actions to be performed like:
Bug Minor change has to be performed on software modules; automation engineer or automation department
manager issue a Software revision request form;
Major change needed on software modules or software modules integration Appropriate documentation has to be
revised to incorporate the requested change and a new version of the involved unit(s) has to be issued.
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Date 16 August 2008
Version 1.4
10. ENCLOSURES
10.1. SOFTWARE REVISION REQUEST FORM ISSUED BY SUPPLIER
10.2. SOFTWARE FEATURE REQUEST FORM ISSUED BY SUPPLIER.
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