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 > Common Quality Assurance Processes and Tools > Software Quality Assurance


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 13th October 2004, 06:08 AM
rstrina rstrina is offline
Inactive Registered Visitor

Registration Date: Sep 2004
Location: Austria, Europe
 
Posts: 7
Thanks Given to Others: 0
Thanked 0 Times in 0 Posts
Karma Power: 21
Karma: 10
rstrina has less than 100 Karma points so far.
Default Advice on OTS software validation

Who could give advice on OFF THE SHELF Software Validation, in particular where and how to find official validation on software provided to the public rather than having to reinvent the wheel so to speak?

Thanks for any hints,
Regards, Renate
Reply With Quote

Sponsored Links
  #2  
Old 20th December 2004, 02:17 AM
Marc's Avatar
Marc Marc is offline
Your Elsmar Cove Host

Registration Date: Jan 1996
Location: West Chester, Ohio - USA
Age: 59
 
Posts: 15,857
Thanks Given to Others: 1,895
Thanked 1,566 Times in 1,018 Posts
Blog Entries: 4
Karma Power: 605
Karma: 11559
Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.
Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.Marc is appreciated, and has over 1700 Karma points.
Send a message via AIM to Marc Send a message via Skype™ to Marc
Default

You mean programs to validate software? What type fo software do you want to validate?
Reply With Quote
Sponsored Links

  #3  
Old 20th December 2004, 05:35 AM
rstrina rstrina is offline
Inactive Registered Visitor

Registration Date: Sep 2004
Location: Austria, Europe
 
Posts: 7
Thanks Given to Others: 0
Thanked 0 Times in 0 Posts
Karma Power: 21
Karma: 10
rstrina has less than 100 Karma points so far.
Default Software Validation hints!

Quote:
Originally Posted by Marc

You mean programs to validate software? What type fo software do you want to validate?
Marc,

Haven't been online for quite some time now, but signed on to find your post. The company I'm working for (MED-EL) is one of the three manufacturer worldwide, who manufacturers a medical device, a cochlear implant, and software is developed for the outside processor to the device.

I have only performed manual testing to the software (system testing), but would like to introduce some automation. Being new to the medical field and being new to automation in software testing, I need to know what the FDA accepts and would isn't allowed?

For any hints or comments, I'd be much obliged!
Sincerely, Renate Strina

SQA, Software Testing
Reply With Quote
  #4  
Old 20th December 2004, 11:14 AM
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

Quote:
Originally Posted by rstrina

Marc,

Haven't been online for quite some time now, but signed on to find your post. The company I'm working for (MED-EL) is one of the three manufacturer worldwide, who manufacturers a medical device, a cochlear implant, and software is developed for the outside processor to the device.

I have only performed manual testing to the software (system testing), but would like to introduce some automation. Being new to the medical field and being new to automation in software testing, I need to know what the FDA accepts and would isn't allowed?

For any hints or comments, I'd be much obliged!
Sincerely, Renate Strina

SQA, Software Testing
www.medel.com
renate.strina@medel.com
This guidance document, General Principles of Software Validation from the FDA may answer your questions.

Do a search in the cove there are other threads, like this one, that discuss this topic.
__________________
Al

Last edited by Al Rosen; 20th December 2004 at 11:28 AM. Reason: added link
Reply With Quote
Reply

Lower Navigation Bar
Go Back   The Elsmar Cove Forum > Common Quality Assurance Processes and Tools > Software Quality Assurance

Bookmarks

Tags
ots, ots software, software


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
Software Validation - Splitting the Level of Concern on multiple software parts SaschaK Medical Devices (21 CFR part 820) 2 5th November 2009 10:39 AM
Quality System Database Validation - FDA's General Principles of Software Validation SpeedRacer24 Qualification and Validation (including 21 CFR Part 11) 11 2nd July 2009 08:59 AM
Drug Product Label Printing Software Validation - PQ Validation erniel Software Quality Assurance 1 16th January 2007 02:00 PM
Software Validation Training - Medical Devices - Seeking advice on outside trainers sherlok Training - Internal, External and Distance Learning 3 30th December 2004 05:57 PM
OTS - Off Tool Sample - APQP xiawas Definitions, Acronyms, Abbreviations and Interpretations 9 17th December 2004 04:45 AM



The time now is 04:14 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