Windows Small Business Server 2003 R2 Overview For Partners
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Transcript Windows Small Business Server 2003 R2 Overview For Partners
Sunday
Business
Systems
The SBS Q-Med Database
Corrective and Preventive Action software for FDA regulated industries
Introduction
Features and Benefits
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Background
Medical Device / FDA Quality standards require many things including:
Corrective Actions
Preventive Actions
Nonconformance dispositions
Internal Audits
Management reviews
Continual Improvement
Customer satisfaction assessments
The SBS Q-Med database was created to ease the complexity of compliance
to quality management system standards:
ISO 13485: Medical devices-Quality management systems-Requirements for
regulatory purposes
Quality System Regulation 21 CFR 820
Electronic Records; Electronic Signatures – CFR 21 Part 11
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Q-Med Database Key Features
Nonconformance Tracking
Escalate a Nonconformance to a Corrective Action
Corrective Actions (CA)
Safety, Supplier, Internal Audit CARs
With Validation and Verification
Approvals require electronic signatures
Preventive Actions (PA)
Audit management
Record audit findings
Manage Audit Schedules
Remedy audit findings with Corrective or Preventive Actions
Meeting management
Project management
Customer satisfaction surveys
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Q-Med Modules
Customer
Complaint
Quality Control
/ Inspection
Non-Conformance
(NCR)
Audits
Surveys
Corrective
Actions (CAR)
Meeting
Manager
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Preventive
Actions (PAR)
Improvement
Projects
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User Interface
Management dashboard for quick assessment
Username and Password protected
Efficient menu system
Data entry in simple forms
A rich set of configurable reports
Email reports with a single click
Easily export data to Excel or Word
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Analysis Tools – Management Dashboard
Quickly assess the
health of
Corrective Actions
Preventive Actions
Nonconformances
Drill down into open
actions for all Types
Easily determine
What is open
Who owns it
And why it’s open
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Analysis Tools
Wide variety of detailed reports
Charts, graphs, Pareto analysis
Quality performance metrics
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General Features
Utilizes the 8D Corrective Action Process
Security with password access and control of privileges
CFR21 part 11 compliant security, Electronic signatures, audit trails
Link electronic documents for a paperless system
Supports single and Multi-user network environments
Built on Microsoft Access 2007
Compatible with Microsoft Access 2010 and 2013
No need to purchase Access if you do not have it
A free run-time version of Access is available from the Microsoft
website
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Benefits
Complies with requirements of
21 CFR 820
ISO 13485
ISO 9001:2008
CFR 21 part 11
Provides a concise, electronic record of historical events, actions, and
improvement
No paper to get lost
Efficiently maintains quality records for
Internal audits
Corrective Action results
Preventive Action results
Management review or MRB meetings
Nonconformances
Customer satisfaction surveys
Improve product reliability and process performance
Improve Customer Satisfaction
Rapidly report results to Customers
Email report directly from the database
Stay on top of key Customer issues
Rebuild customer confidence when things go wrong
Analyze Customer perceptions over time
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Benefits
Efficient and cost effective
Simple, low cost solution
No additional software to purchase
No annual maintenance fees
Concurrent user licensing – not CPU based
Minimal training is required
Saves time and improves efficiency
Reports and analysis
Managers get immediate answers
How many CA/PA Requests are open and why?
How long are CA/PA Requests open?
Email reminders for open actions
Develop agendas for meetings
Easy to identify and manage open action items
Reduce cycle time to implement corrective actions
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Login Screen
The login process limits access to the database features
The Demo version includes dummy data and employees
administrator has full Database privileges
For the demo database,
– Username: administrator
– Password: Aa777777
– Note: username and password are case sensitive
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Corrective Action Requests
Background: The 8D problem solving process
CAR Form
Reports and analysis
Measure effectiveness
The 8D Problem Solving Process
D0
• Plan
D1
• Build a team
D2
• Define the problem
D3
• Contain the problem
D4
• Define and verify the root cause(s)
D5
• Determine and verify the permanent corrective actions
D6
• Implement and verify the permanent solution
D7
• Prevent recurrence
D8
• Congratulate the team!
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CAPA Life Cycle
Action
Description
Status
State
New CAR or PAR
Started a new CAR or PAR
Waiting
Containment
Open
Implement
Containment Actions
Containment actions were devised
and effectively implemented
Containment
Complete
Open
Develop corrective
and / or preventive
actions
The CAPA plan was developed and
approved (e-Sig)
Plan Approved
Open
Complete CAPA
All corrective and Preventive
actions complete and validated
Complete
Closed
Final Review and
Approval
Review CAR / PAR; e-Sig required
for final approval
CLOSED &
Approved
Closed
Place CAR or PAR on
Hold
On Hold
Open
Cancel CAR or PAR
Cancelled
Closed
Exceptions
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Corrective Action Form
Form is organized
into 6 tabs
Yellow fields are
required fields
Purple fields
indicate Electronic
Signatures
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Corrective Action Form - Containment
Establish
containment actions
with specific owners
Electronic signature
required to approve
containment
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Corrective Action Form – Root Cause Analysis
Ask why? Enough times to
determine effective root causes
Document multiple root causes for a
single CAR including Primary, Escape,
and Contributing root causes
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Corrective Action Form – Corrective Actions
Establish clear,
quantifiable
acceptance criteria
Electronic signature
required to approve
validation
Electronic signature required
to approve Root
Cause/Corrective Action Plan
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Corrective Action Life Cycle
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Corrective Action Form – Preventive Actions
Electronic signature
required to approve
Preventive Action plan
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Corrective Action Form – Comments and Attachments
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Corrective Action Report
Print or email the CAR report directly to the Customer
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Reports and Analysis
Rich set of reports including Pareto graphs and trend charts
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Preventive Actions
PAR Form
Reports and analysis
Measure effectiveness
For want of a nail, the shoe was lost,
For want of the shoe, the horse was lost,
For want of the horse, the rider was lost,
For want of the rider, the battle was lost,
For want of the battle, the kingdom was lost,
And all for the want of a horseshoe nail!
Preventive Actions
PARs are handled nearly the same as CARs
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PAR Reports
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Nonconformance Tracking
Track non-conformances
Failure Analysis
Analyze defects for continual improvement
Escalate a Nonconformance to a CAR
Nonconformance Tracking
Enter General
Nonconformance details
Classify the
Nonconformances
based on the defect
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Failure Analysis
Describe the failure analysis
technique and results
Assign multiple root causes –
later, analyze by root cause
Produce professional Failure
Analysis reports
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Disposition
Document what is to be done
with the material: Release,
Rework, Downgrade, or Scrap
Produce a concise
nonconformance report
Escalate any Nonconformance to a CAR
with a click of a button
Electronic Signature
required to approve
Material Disposition
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Actions associated with the NC
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Nonconformance Analysis
Rich set of configurable reports and charts
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Audit Management
Maintain audit schedules
Document audit findings
Convert findings into a CAR and / or PAR
Report and analyze results
Audit Details
Electronic Signature
required to approve and
close Audit
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Audits Findings
Document detailed
audit findings
Create a CAR or PAR
Linked to the Audit with
a click of a button
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Audit Conclusions
Summarize Strengths,
Weaknesses, and
overall Conclusions
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Audit documentation
Add all supporting
documentation
(electronic files)
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Audit Report
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Manage Audit Schedule
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Audit Reports and Analysis
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Meeting Manager
Document meeting minutes
Track and manage actions
Drive Continual Improvement at the management level
Background
Great for MRB and Quality Management System Review meetings
Document a meeting
Who attended
What was the agenda?
What was discussed?
What were the resulting actions to be taken?
Are the actions complete?
Were the actions effective?
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Meeting Details
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Meeting Minutes
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Actions and Validation
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Supporting documents
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Surveys
Create Customer Satisfaction surveys
Create Vendor Qualification surveys
Manage & analyze survey results
Simple Survey Features
Easily create custom surveys
Simple, intuitive interface
Print out or e-mail a professional looking survey directly
from the program
Ask different types of questions
True or False / Yes or No
Rating (on a scale of one to ten)
Text response (let the customer provide feedback in his own
words)
Create an efficient quality record
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Simple Survey Features
Customer Satisfaction
Directly quantify customer satisfaction
Monitor Customer perceptions
Analyze trends with grafts and reports
Vendor qualification surveys
Measure vendor suitability
Monitor vendor improvement
Employee opinion polls
Measure job satisfaction
Solicit continual improvement ideas
Measure and track long term results print
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Create a Survey
Simple, efficient interface
Enter General
Information
Data entry in simple forms
Organize the
survey into topics
List all Survey
questions & define
types
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Creating Surveys
Enter general survey information
Create a survey Category (i.e. Customer Service, General, Engineering Support, etc.)
Create a question and establish the order in which it will appear on the survey
Select the question type.
Yes/no and true/false questions are rated as either 0 or 10
Text response questions have no score
Rating types receive a number rating from 1 to 10 with 1 being the lowest or worst level.
If the question was yes/no or true/false, you must determine if a positive answer
(yes or true ) carries the maximum score.
Check the check box labeled "PositiveIsTen" if a positive answer receives the maximum
score.
Leave the "PositiveIsTen" check box unchecked if a positive answer should receive the
minimum score.
Each question may be weighted differently (not all questions were created equal).
The "Weight" field is used to score each question where Score = Rating * weight.
The user must determine appropriate waiting factors.
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Produce Professional Looking Surveys
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Survey Analysis Tools
Variety of customizable reports
Charts, graphs
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SBS Q-Med Database
Configuration and Installation
Demo Database Installation
The demo database is a stand-alone access database with all the features of
the standard product.
To install the program:
Download the demo database from www.SundayBizSys.com
Save or copy the Q-Med Database.accde file to a designated folder on your
Network File Server
Ensure all Workstations have
Microsoft Access or the free Runtime version of Microsoft Access
Read and write privileges to the designated folder on the Network File Server
Note: The above graphic is for stand alone Access databases - SQL configurations are different
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Purchased Product Installation
The purchased product has 2 parts:
Microsoft SQL back end
Microsoft Access front end
The Microsoft Access front end connects to the SQL back end through
standard ODBC links from each user computer.
The Customer must provide the SQL server and the database
administration. SBS will provide the SQL files for installation and the Q-Med
front end.
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SBS Q-Med Database
Best in class software solution
Summary
The SBS Q-Med Database is a cost effective tool to
Ensure effective compliance with Quality standards
ISO 13485
21 CFR 820 - Quality System Regulation
21 CFR Part 11
ISO 9001:2008
Manage meetings
Monitor Customer perceptions
Maintain paperless quality records
Analyze performance and develop improvement strategies
Save time and effort
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About SBS
Sunday Business Systems is engaged in software sales and consulting
services.
Sells affordable and efficient software solutions to implement Quality
management systems:
Document Control
Corrective and Preventive Actions
Audit Management
Employee Training
Control of calibrated equipment
Vendor Management
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Business
Systems
SPC
Continual improvement
Provides Training and instruction
Provides custom software solutions
Modify and existing program
Build a complete custom solution for your specific business processes
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Sunday
Business
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Fueling Small Business Efficiency
Visit www.SundayBizSys.com for:
•Additional information
•Free product demos
•Pricing
•Links to purchase software
© 2014 Sunday Business Systems. All rights reserved. This presentation is for informational purposes only. Sunday
Business Systems MAKES NO WARRANTIES, EXPRESS OR IMPLIED, IN THIS SUMMARY. Microsoft is a
registered trademark of Microsoft Corporation in the United States and/or other countries.