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 > Medical Devices, Medical Information Technology, Medical Software and Health Informatics > Medical Device Related Regulations > US Medical Device Regulations > US Medical Devices (21 CFR part 820)
Forum Username


Elsmar Cove Forum Sidebar
Custom Search
Monitor the Elsmar Forum
Monitor New Forum Posts
Follow Marc & Elsmar
Elsmar Cove Forum RSS Feed  Marc Smith's Google+ Page  Marc Smith's Linked In Page   Marc Smith's Elsmar Cove YouTube Page  Marc Smith's Facebook Page
Elsmar Cove Groups
Elsmar Cove Google+ Group  Elsmar Cove LinkedIn Group  Elsmar Cove Facebook Group
Sponsor Links







Donate and $ Contributor Forum Access
Sponsored Links
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

Marcelo Antunes'
SQR Consulting

Bob Doering's
Correct SPC - Precision Machining


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


Related Topic Tags
fda (food and drug administration), unique identification (uid)
Reply
 
Thread Tools Search this Thread Rate Thread Content Display Modes
  #17  
Old 9th May 2013, 01:35 PM
lboll lboll is offline
Involved in Discussions

 
Registration Date: Apr 2009
Location: USA
 
Posts: 19
Thanks Given to Others: 2
Thanked 5 Times in 1 Post
Karma Power: 18
Karma: 35
lboll has less than 100 Karma points so far.
Re: US FDA Unique Device Identification (UDI) Proposed Rule

Thanks, Karen! I hadn't seen that. There's hope yet.

Sponsored Links
Reply

Lower Navigation Bar
Go Back   The Elsmar Cove Forum > Medical Devices, Medical Information Technology, Medical Software and Health Informatics > Medical Device Related Regulations > US Medical Device Regulations > US Medical Devices (21 CFR part 820)

Do you find this discussion thread helpful and informational?


Bookmarks


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

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

Forum 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


Similar Discussion Threads
Discussion Thread Title Thread Starter Forum Replies Last Post or Poll Vote
Unique Document Identification Numbering System NarayanMalladi Documentation Control Systems, Procedures, Forms and Templates 59 27th July 2010 12:54 AM
US FDA Proposed Rule for Combination Product Reporting bio_subbu US Food and Drug Administration (FDA) 1 6th October 2009 10:23 AM
FDA's Unique Device Identification, New Regulations - Pending March of 2010 Quality96 - 2011 ISO 13485 and ISO 14969 - Medical Devices - Quality Management Systems 3 21st July 2009 11:11 AM
FDA Unique Device Identifiers on the labeling of devices MIREGMGR US Medical Devices (21 CFR part 820) 3 10th February 2009 04:44 PM
Where traceability is required, the unique identification of the product is recorded Juris ISO 9000, ISO 9001, and ISO 9004 - Questions and Discussions 4 13th November 2007 10:12 AM



The time now is 10:53 AM. All times are GMT -4.
Your time zone can be changed in your UserCP --> Options.


   


Marc Timothy Smith - Elsmar.com
8466 LeSourdsville-West Chester Road, West Chester, Ohio 45069-1929
513 341-6272