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Showing results 1 to 35 of 44 This Search took 0.02 seconds to complete. Search: Posts From the Last 24 Hours (Rolling)
	Discussion Thread Title / Thread Starter	Last Post or Poll Vote	Replies	Views	Forum
	Bad news/good news day ( 1 2 3) Colpart started this discussion on 20th November 2009	23rd November 2009 10:32 AM by Migre	16	257	Coffee Break and Water Cooler Discussions
	Consumable Parts Monitoring and Reordering - Gloves, grinding discs, earplugs, etc. ( 1 2) palmer started this discussion on 13th October 2009	23rd November 2009 10:30 AM by palmer	8	390	Lean - Lean in Manufacturing and Services
	CQI (Chartered Quality Institute, UK) - Diploma in Quality ( 1 2) Phiobi started this discussion on 2nd February 2009	23rd November 2009 10:05 AM by achorste	12	607	Professional Certifications and Degrees
	UL 508C section 44 - what does it say? smryan started this discussion on 20th November 2009	23rd November 2009 10:04 AM by smryan	2	102	Various Other Specifications, Standards, and related Requirements
	Interesting article - Analysis of Risk: Are Current Methods Theoretically Sound? mmantunes started this discussion on 20th November 2009	23rd November 2009 10:03 AM by icare2much	1	92	ISO 14971 - Medical Device Risk and Hazard Control
	AS9100 Awareness Training Al Rosen started this discussion on 23rd November 2009	23rd November 2009 10:00 AM by BadgerMan	1	37	AS9100 Aerospace Standard and Requirements
	More Registrar Consolidation: UL and DQS to merge. ( 1 2 3) Sidney Vianna started this discussion on 1st April 2008	23rd November 2009 09:45 AM by Cem Onus	18	2,372	Registrars (Certification Bodies) and Registration
	Internal Audit Procedure and Schedule example Sweetsue28uk started this discussion on 23rd November 2009	23rd November 2009 09:42 AM by Ted Schmitt	2	63	Internal Auditing
	Updating Certificate of Foreign Government (CFG's) ( 1 2) markvm68 started this discussion on 9th September 2009	23rd November 2009 09:29 AM by MIREGMGR	12	385	ISO 13485 - Medical Devices - Quality Management Systems
	Acceptable Criteria for Variable Gage R&R aproddutoor started this discussion on 23rd November 2009	23rd November 2009 09:24 AM by aproddutoor	0	34	Gage R&R (GR&R) and MSA (Measurement Systems Analysis)
	Missed Quarterly Dose Audit! Sterilization Validation of Medical Devices ( 1 2) Tara QA started this discussion on 16th November 2009	23rd November 2009 09:23 AM by jscholen	11	334	ISO 13485 - Medical Devices - Quality Management Systems
	Radiation Survey per AMS2750D - Looking for a supplier Ontario/Quebec sorin started this discussion on 23rd November 2009	23rd November 2009 08:54 AM by sorin	0	47	Manufacturing and Related Processes
	Zombie Requirements - Registrar's auditors have yet to get IAQG-designed training John Broomfield started this discussion on 18th November 2009	23rd November 2009 08:52 AM by BadgerMan	1	102	AS9100 Aerospace Standard and Requirements
	Quality Systems Coordinator vs. Management Representatve - Responsibilities and Roles jeanmarc started this discussion on 23rd November 2009	23rd November 2009 08:42 AM by tkevmoore	2	73	ISO 9001 - Quality Management Systems Standard
	Inquiry about the number of changes in a document TarKEpa started this discussion on 22nd November 2009	23rd November 2009 07:45 AM by mzeeshanz	5	114	Documentation Control Systems, Procedures, Forms and Templates
	CAR to Assessor - Is it allowed to issue a corrective action to an assessor? ( 1 2 3) selena15 started this discussion on 20th October 2009	23rd November 2009 07:37 AM by AndyN	21	536	ISO 19011 and ALL Auditing Discussions
	European Borderline Product Guidelines Version 1.5 - Medical Devices bio_subbu started this discussion on 23rd November 2009	23rd November 2009 07:33 AM by chris1price	1	43	CE Marking (Conformité Européene) / CB Scheme
	For Sale: QCI SSBB Primer QE started this discussion on 1st November 2009	23rd November 2009 07:20 AM by bob5621	2	117	Buy, Sell or Trade - NO Commercial Advertisements
	MDD and Mandatory Standards (IEC/EN 60601-1-4, 60601-1-6 and ISO 14971) LievenDW started this discussion on 16th November 2009	23rd November 2009 05:13 AM by Peter Selvey	6	180	CE Marking (Conformité Européene) / CB Scheme
	Electrosurgical Testing - Is there a specific standard for Electrosurgical Testing? nikolaos started this discussion on 20th November 2009	23rd November 2009 05:05 AM by nikolaos	4	129	IEC 60601 - Medical Electrical Products Collateral Standards
	Standard Version(s) on Declaration of Conformity (DoC) - Necessary or required? Jwreeves started this discussion on 20th November 2009	23rd November 2009 04:58 AM by Peter Selvey	2	111	CE Marking (Conformité Européene) / CB Scheme
	Introduction of SPC - Embarking on my first implementation for precision machining UK Steve started this discussion on 22nd November 2009	23rd November 2009 04:47 AM by UK Steve	4	91	SPC Monitoring and Statistical Analysis Techniques
	FAQ Thread: New Folks - Please Take a Minute and Introduce Yourself/Say Hello! Take 2 (2009) ( 1 2 3 4 5 6 ... Last Page) Greenraisin	23rd November 2009 04:12 AM by Jeffg67	63	2,074	Coffee Break and Water Cooler Discussions
	Internal Audit Finding - Root Cause Analysis: Auditor or an Auditee Responsibility? ( 1 2 3) dQApprentice started this discussion on 19th November 2009	23rd November 2009 04:04 AM by anil123	21	374	Internal Auditing
	Notified Body on Class I Declaration of Conformity? Jwreeves started this discussion on 16th November 2009	23rd November 2009 03:48 AM by Jerome	4	136	CE Marking (Conformité Européene) / CB Scheme
	What is the appropriate number of NC (Nonconformances) for this case? ( 1 2 3 4 5) dQApprentice started this discussion on 16th November 2009	23rd November 2009 03:12 AM by JaneB	34	651	Nonconformance and Corrective Action
	Top Management & Improvement Processes ( 1 2 3) D.Salman started this discussion on 18th November 2009	23rd November 2009 02:55 AM by JaneB	22	450	Quality Tools, Improvement and Analysis
	Breakdown and Analysis of FDA Warning Letters Fifi2006 started this discussion on 11th November 2009	23rd November 2009 02:55 AM by Nikunj	6	206	FDA (United States Food and Drug Administration)
	Use of Phthalates (PVC) - MDD 2007/47/EC - Has anyone started labelling devices ( 1 2 3) SteveK started this discussion on 24th December 2008	23rd November 2009 12:13 AM by Peter Selvey	19	2,944	CE Marking (Conformité Européene) / CB Scheme
	Control of Outsourced Processes (not properly described in the quality manual) ( 1 2 3) Edugar started this discussion on 15th October 2009	22nd November 2009 11:54 PM by Peter Selvey	17	1,040	ISO 13485 - Medical Devices - Quality Management Systems
	Gage R&R - How do I know my gauge is in specification - Repeatability Devlin started this discussion on 22nd November 2009	22nd November 2009 09:48 PM by Devlin	0	73	Gage R&R (GR&R) and MSA (Measurement Systems Analysis)
	How many records should I keep when implementing Corrective Actions QAMTY started this discussion on 22nd November 2009	22nd November 2009 09:42 PM by Stijloor	1	74	Records and Data - Quality, Legal and Other Evidence
	Validation - The process or product? ISO 9001 Clause 7.3.6 ( 1 2 3) QAMTY started this discussion on 4th November 2009	22nd November 2009 08:48 PM by Big Jim	16	548	ISO 9001 - Quality Management Systems Standard
	"Value" and "Overhead(s)" of implementation of "CSV - Validation requirements" v9991 started this discussion on 21st November 2009	22nd November 2009 07:31 PM by mmantunes	1	100	Qualification and Validation (including 21 CFR Part 11)
	SOX (Sarbanes-Oxley Act) within an organization selena15 started this discussion on 17th November 2009	22nd November 2009 03:40 PM by selena15	6	162	Forum News and General Information
Showing results 1 to 35 of 44

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