Understanding Validation of Production & Service Provision


Understanding Validation of Production & Service Provision

Understanding Validation of Production & Service Provision

E-mail this product to a friend E-mail this product to a friend


Previous  Up  Next" 

DATES & TIMES
August 12, at 1:00 p.m. EDT | 10:00 a.m. PDT
Please check your time zone for the correct local time


LENGTH
One hour

PRICE
$199

 
SUMMARY
From the time ISO 9001 was revised in 2000 to the time the most recent revision, there has been confusion on what processes need to be validated according to the requirements in clause 7.5.2, Validation of processes for production and service provision. This is further complicated by organizations that confuse the validation associated with design to the validation of processes. If you struggle with understanding these requirements, this webinar will help you.


Topics to be discussed include:
  • What validation of processes is and is not
  • Reviewing examples in the manufacturing and service industry
  • Applying the requirements of 7.5.2 to manufacturing and service examples

After this webinar, attendees will understand the requirements in ISO 9001:2008 clause 7.5.2 in a manner to ensure they have effectively implemented them. It will also provide details on any adjustments you might need to make to your current quality management system. This information will help your organization sustain and continually improve its quality management system.


DETAILED COURSE AGENDA
  • Validation of Processes for Production and Service Provision     
    • What it Is vs. What it is Not
      • IS - Validation of Processes that cannot be verified during subsequent monitoring or measurement.
      • IS NOT - Validation of Processes to ensure that they are documented correctly.
    • ISO 9000 Definitions
      • Verification
      • Validation
    • Taking an Exclusion
  • Examples of Processes that cannot be verified by subsequent monitoring or measurement
    • Manufacturing Examples
    • Service Industry Examples
  • Review requirements of 7.5.2 in context of manufacturing and service industry examples.
    • How to define criteria for review and approval
    • Approval of Equipment
    • Qualification of Personnel
    • Use of specific Methods and Procedures
    • Required Records
    • Re-Validating the Process
  • Summary
  • Questions and Answers


BONUS
Get your specific questions answered in a live Q&A session during the webinar.

 
PRESENTER

Lorri Hunt has over 13 years of experience in implementing quality management systems in diverse organizations. While employed by Honeywell, she assisted many subsidiaries within the corporation and the Department of Energy, National Nuclear Security Administration with ISO 9001 implementation. She has also worked with small organizations through the New Mexico 9000 program. Through this program she has provided training and coached over 100 organizations on ISO 9001 tools, techniques, and methods that will sustain their organization after the engagement is complete.

Lorri Hunt is an active member of the U. S. Technical Advisory Group to ISO Technical Committee 176. She currently serves in the key position of Chair of Task Group 9001/4, the United States group responsible for developing consensus positions related to ISO 9001 and 9004. Recognized internationally as someone who gets the job done, she has held several international positions on ISO TC176. Most recently she was appointed as the Deputy Task Group Leader to the current amendment to ISO 9001.

Lorri frequently contributes to quality publications and journals and was a contributing author to the ISO 9000:2000 Handbook. She is a frequent speaker at conferences.

Lorri is most often recognized for using her 10 years of experience to assist organizations in implementing ISO 9001:2000 using a common sense approach. She is the president of Lorri Hunt and Associates Inc..

 
 
HOW DOES THIS ALL WORK?
After you register for the Webinar, you will receive a confirmation e-mail. It will contain a Web link to access the visual portion of the event through your Web browser. It will also contain an a phone number and access code that you will use to hear the audio portion of the event.
 
 
PROGRAM MATERIALS
Program materials will be provided approximately three days before the program date via email with PDF links. Please download the PDF files before the day of the program. If you register for the event less than three days before it is scheduled to begin, you will receive the course materials via e-mail shortly after you register.
 
 
PRICING
We are so confident that you will find this webinar valuable that we offer a 100% money back guarantee, making this a risk-free investment. If you are dissatisfied with the webinar, just let us know by phone or e-mail within 24 hours of the conclusion of the webinar, and we will issue you a full refund.
 

PLEASE NOTE: Participation in this webinar is just $199 per site and allows access to ONE Internet connection and ONE phone line. You must provide a valid e-mail address in order to receive the e-mail confirmation and materials. If your organization blocks third-party e-mails, you might want to use a personal e-mail address to be sure you receive the information. Usually when participants tell us that they have not received our e-mails, it is because they have either been blocked by their company or their spam filter.

Price: $199.00 


Quantity:  

Enter number of participants above and the name and e-mail of each PAID participant below:

 

Making the Most of Your Quality Manual
Making the Most of Your Quality Manual
Procedure Writing
Procedure Writing
The Insiders' Guide to ISO 9001:2008
The Insiders' Guide to ISO 9001:2008
Calibration: What Auditors Look for in a Controlled Process
Calibration: What Auditors Look for in a Controlled Process