ISO 13485 and ISO 14969 - Medical Devices - Quality Management Systems

		The Elsmar Cove Forum > Medical Devices, Medical Information Technology, Medical Software and Health Informatics > Medical Device Related Standards
ISO 13485 and ISO 14969 - Medical Devices - Quality Management Systems

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ISO 13485 and ISO 14969 - Medical Devices - Quality Management Systems - Discussion Threads

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Rating Discussion Thread Title / Thread Starter	Last Post or Poll Vote	Replies	Views
Use of Antimicrobial Inhibitors in Medical Devices ( 1 2) WisdomseekerSC started this discussion on 13th November 2009	19th November 2009 05:04 PM by MIREGMGR	10	1,479
Changing a UK Notified Body - Anyone with any experience? ( 1 2 3) Dave-h started this discussion on 23rd July 2004	12th December 2009 06:07 PM by bergamo	22	4,822
ISO 13485:2003 QMS Flow - I have just put together my first draft ( 1 2) compliance - 2006 started this discussion on 10th November 2004	24th November 2009 05:32 PM by Al Rosen	15	3,600
Scope for ISO 13485 vs. ISO 15378 - Molding Parts for Medical Devices Ajit Basrur started this discussion on 11th September 2007	31st December 2009 04:38 AM by sharadmshukla	4	4,319
Guidance on ISO 13485 Section 7.5.2. about Software Validation ( 1 2) Padams13 started this discussion on 21st November 2007	22nd December 2009 08:42 PM by vinh_lex - 2010	15	4,589
Veterinary device is medical device or not? ( 1 2) luloo117117 started this discussion on 31st December 2008	14th December 2009 11:47 AM by Aaron Lupo	11	3,024
Practical Reasons Behind The ISO 13485/QSR Regulations Mark M. Sweeny started this discussion on 26th June 2009	8th December 2009 04:03 PM by swiffy	6	1,171
Symbol or Label requirements for "Demo Instrument"? sreenu927 started this discussion on 14th November 2009	17th November 2009 10:51 PM by sreenu927	4	1,250
How to document rework being completed at Suppliers on Medical Devices? christophermix started this discussion on 17th November 2009	18th November 2009 11:26 AM by christophermix	3	1,059
ISO 10993-1:2009 incorporating Risk Management published by ISO RA Princess started this discussion on 17th November 2009	17th November 2009 06:40 AM by Marcelo Antunes	1	2,576
Supplier Re-evaluation Methods ( 1 2) maxwell started this discussion on 25th November 2009	29th November 2009 08:07 PM by Stijloor	8	2,121
EN ISO 13485 vs ISO 13485 Certification - EN vs EN ISO Differences ( 1 2) icare2much started this discussion on 25th November 2009	14th December 2009 12:40 PM by icare2much	12	4,129
Considering adding ISO 13485 certification - Your thoughts? rlsavard started this discussion on 4th December 2009	4th December 2009 08:34 AM by somashekar	4	891
Supplier Audit - Help me with some examples of supplier audit templates romit singh started this discussion on 7th December 2009	8th December 2009 12:00 AM by harry	6	3,193
Language requirements in Malaysia - What language the IFUs need to be in Burgmeister started this discussion on 10th December 2009	13th December 2009 05:28 AM by harry	5	1,273
Recording Scrap - Problems in the Medical Device Manufacturing Sector excellerator started this discussion on 11th December 2009	14th December 2009 08:13 AM by Marc	4	1,075
Linked: CAPA - Process - Class III Medical Device Manufacturing QE started this discussion on 11th December 2009	-	-	-
Linked: Record Retention Log - What Records are required in a Record Retention Log Swiss22 started this discussion on 15th December 2009	-	-	-
Linked: Paperless Document Control System - Recommendations needed WisdomseekerSC started this discussion on 16th December 2009	-	-	-
Linked: Non-Conformance Procedure FlowChart for a Medical Device company romit singh started this discussion on 29th December 2009	-	-	-

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ISO 13485 and ISO 14969 - Medical Devices - Quality Management Systems

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