The Elsmar Cove Forum and Site Map The Elsmar Cove Wiki More Free Files The Elsmar Cove Forums Discussion Thread Index Post Attachments Listing Failure Modes Services and Solutions to Problems Elsmar cove Forums Main Page Elsmar Cove Home Page

Go Back   The Elsmar Cove Forum > ISO (International Organization for Standardization) Standards > ISO and IEC Medical Device Related Standards > ISO 13485 - Medical Devices - Quality Management Systems


The Elsmar Cove Forum SideBar!
Monitor the Forum
Monitor New Forum Posts
New Threads Feeds
RSS FeedRSS Feed
Sponsor Link










$ Contributor Forum Access
Courtesy Quick Links

Links that Elsmar Cove visitors will find useful in your quest for knowledge:


Howard's International Quality Services

Atul's Symphony Technologies

Dave Scott's Scott Quality Solutions

Praxiom Research Group


NIST's Engineering Statistics Handbook

IRCA - International Register of Certified Auditors

SAE - Society of Automotive Engineers

Quality Digest Portal

IEST - Institute of Environmental Sciences and Technology

ASQ - American Society for Quality


All the Important Standards and Related Web Sites in the World
Reply
 
Thread Tools Search this Thread Rate Thread Content Display Modes
  #1  
Old 17th March 2004, 01:00 PM
DJIND DJIND is offline
Inactive Registered Visitor

Registration Date: Mar 2004
Location: New Jersey
 
Posts: 3
Thanks Given to Others: 0
Thanked 0 Times in 0 Posts
Karma Power: 24
Karma: 10
DJIND has less than 100 Karma points so far.
Default Iso 13485 Procedures

Hello, I'm hoping someone can help. I was all set for our final audit for ISO 9000 when a new customer requested ISO 13485. We have no customers requiring us to get ISO9000 so we postponed the final audit. We are a small manufacturing company and our budget has been used for the ISO 9000. I have all our Procedures for ISO9000 and I was wondering if any one has general procedures for ISO 13485 that I can use as a template. Any help would be greatttly appreciated.

Thanks
Reply With Quote

Sponsored Links
  #2  
Old 17th March 2004, 01:51 PM
Kevin Mader's Avatar
Kevin Mader Kevin Mader is offline
One of THE Original Covers!

Registration Date: Nov 1998
Location: Wallingford, CT USA
Age: 43
 
Posts: 1,158
Thanks Given to Others: 22
Thanked 63 Times in 43 Posts
Karma Power: 94
Karma: 1335
Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.Kevin Mader is appreciated, and has over 1300 Karma points.
Send a message via AIM to Kevin Mader
Default

Hello DJIND,

Welcome to the Cove!!

Have you reviewed the requirements under 13485?

Regards,

Kevin
__________________
"Without theory there is nothing to modify or learn." W. Edwards Deming
Reply With Quote
Sponsored Links

  #3  
Old 17th March 2004, 02:53 PM
DJIND DJIND is offline
Inactive Registered Visitor

Registration Date: Mar 2004
Location: New Jersey
 
Posts: 3
Thanks Given to Others: 0
Thanked 0 Times in 0 Posts
Karma Power: 24
Karma: 10
DJIND has less than 100 Karma points so far.
Default

Kevin,

Hi. Thanks for replying. I am currently in the process of re-writing our quality manual so it conforms to ISO 13485, so I am reviewing the requirements as I'm rewriting.

Diana
Reply With Quote
  #4  
Old 17th March 2004, 03:29 PM
DannyK DannyK is offline
Involved - Posts

Registration Date: Jul 2003
Location: CANADA
 
Posts: 318
Thanks Given to Others: 29
Thanked 89 Times in 68 Posts
Karma Power: 50
Karma: 907
DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.DannyK is appreciated, and has over 900 Karma points.
Default

Hi

Are you talking about ISO 13485:1996 or ISO 13485:2003?

I think the best way to go about modifying your manual and procedures is by doing a gap analysis and identifying what is missing.

Danny
Reply With Quote
  #5  
Old 17th March 2004, 03:53 PM
DJIND DJIND is offline
Inactive Registered Visitor

Registration Date: Mar 2004
Location: New Jersey
 
Posts: 3
Thanks Given to Others: 0
Thanked 0 Times in 0 Posts
Karma Power: 24
Karma: 10
DJIND has less than 100 Karma points so far.
Default

Danny,

Hi. Thanks for replying. I am currently re-writing our manual to the ISO 13845:2003 and at the same time trying to identify what's missing. I downloaded from this site an Audit checklist which highlights the differences between ISO 9001:2000 and ISO 13485:2003 which I believe will help.

Thanks
Diana
Reply With Quote
  #6  
Old 17th March 2004, 05:43 PM
liuyy liuyy is offline
Involved in Discussions

Registration Date: Mar 2004
Location: BEIJING,CHINA
 
Posts: 23
Thanks Given to Others: 0
Thanked 5 Times in 3 Posts
Karma Power: 27
Karma: 172
liuyy is appreciated, and has over 100 Karma points.liuyy is appreciated, and has over 100 Karma points.
Please Help!

Hi,Diana,

If you try ISO 13485:2003,more procedures are needed than ISO 13485:1996.At the same time,risk management through the whole product realization processes required in 7.1 of ISO 13485:2003 needs much more documents and records from you than just a risk analysis documentation in design process as required in 4.4.1 of ISO 13485:1996.

Liuyy
Reply With Quote
  #7  
Old 17th March 2004, 06:17 PM
Al Rosen's Avatar
Al Rosen Al Rosen is offline
Forum Moderator

Registration Date: Jun 2002
Location: Lawn Guyland
Age: 59
 
Posts: 3,101
Thanks Given to Others: 48
Thanked 390 Times in 272 Posts
Karma Power: 192
Karma: 4968
Al Rosen is appreciated, and has over 1700 Karma points.
Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.Al Rosen is appreciated, and has over 1700 Karma points.
Send a message via AIM to Al Rosen
Default

Hi Diana,

Have you searched the cove for other threads? I placed a link to a web site that has templates, in this thread http://elsmar.com/Forums/showthread.php?t=8098
__________________
Al
Reply With Quote
Reply

Lower Navigation Bar
Go Back   The Elsmar Cove Forum > ISO (International Organization for Standardization) Standards > ISO and IEC Medical Device Related Standards > ISO 13485 - Medical Devices - Quality Management Systems

Bookmarks


Visitors Currently Viewing this Thread: 1 (0 Registered Visitors and 1 Unregistered Guests)
 
Thread Tools Search this Thread
Search this Thread:

Advanced Forum Search
Display Modes Rate Thread Content
Rate Thread Content:

Posting Settings
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump

Similar Discussion Threads
Discussion Thread Title Thread Starter Forum Replies Last Post or Poll Vote
Any examples of the required ISO Procedures for a small Recruitment Company Hurgate Documentation Control Systems, Procedures, Forms and Templates 7 7th July 2008 09:51 AM
13485:2003 7.5.3 and 8.4 - Seeking examples of procedures needed for these clauses t845526 ISO 13485 - Medical Devices - Quality Management Systems 4 9th November 2005 12:02 PM
Good Manufacturing Procedures and SSOP - Seeking Examples peter_pan__ ISO 22000, HACCP (21 CFR 120) and Food Safety 2 17th July 2005 10:03 PM
MRP / ERP Software Systems - Small medical laser manufacturing company - ISO 13485 janiswilson Quality Assurance and Compliance Software Tools / Solutions 6 7th October 2004 04:00 PM
Implementation of ISO 9000 in a small manufacturing company mikorfa ISO 9001 - Quality Management Systems Standard 4 26th July 2001 09:48 PM



The time now is 03:05 AM. All times are GMT -4.
The time zone can be changed in your UserCP --> Options.



   

All Y'All Come Back Now, Y' Hear?

Made With A Mac! FreeBSD OS Powered by Apache!
Using php4 Forums provided and maintained by Marc Smith Database by MySQL

FAIR USE and CORRECTNESS NOTICE: This site contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available in our efforts to advance understanding of environmental, political, human rights, economic, democracy, scientific, and social justice issues, etc. We believe herein constitutes a 'fair use' of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, the material on this site is distributed without profit to those who have expressed a prior interest in receiving the included information for research and educational purposes. For more information go to: http://www.law.cornell.edu/uscode/17/ If you wish to use copyrighted material from this site for purposes of your own that go beyond 'fair use', you must obtain permission from the copyright owner. In addition, I do not guarantee the correctness of the content. The risk of using content from the Elsmar Cove web site and forums remains with the user/visitor.

Responsibility Statement: Each person is responsible for anything they post in the Elsmar Cove forum. Neither I, Marc Timothy Smith, nor any of the forum Moderators, are responsible for the content of posts people make. Liability for post content resides with the poster as does interpretation and/or acceptance and/or use of advice by the reader.

Complaints: If you have a complaint with a post in a forum discussion thread, including Content in general, fighting, flaming, copyright infringement, defamation and/or 'slander', please use the 'Report This Post Report This Post Button button which appears at the top of every post in every thread.

Site courtesy of:
Marc Timothy Smith - Cayman Business Systems, 8466 Lesourdsville-West Chester Road, West Chester, Ohio 45069-1929 - USA
(513) 341-6272

To contact me, click the Google Voice link below, enter Your Name and Your Phone Number and Google will ring your phone and connect you for free!

The Elsmar Cove Web Site is *CopyFree*
no new posts