The Elsmar Cove Forum > ISO (International Organization for Standardization) Standards > ISO 19011 and ALL Auditing Discussions

Pages : [1] 2 3

1. Want To Be A 'Certified' Lead Auditor? A discussion
2. The Albatross
3. ISO 10011 Status - OBSOLETE STANDARD
4. Tools of the Auditing Trade
5. The Art of Auditing Calibration - The most common nonconformances found
6. Lead Assessor 5 day course
7. Lead Auditor Class is Over (At Last)
8. Training of Internal Quality Auditors - Over all the aspects of ISO10011 Parts 1 & 2?
9. Semiconductor supplement
10. Internal Quality Auditors training
11. Audit Man-days - And Other Charlie Thoughts
12. Advice for Auditors /Scalies
13. Auditing for effectiveness
14. World's Funniest Audit Experiences
15. Getting the Most out of Internal Audits - Confirming to Innovating
16. Input - Joint Auditing Standard
17. ISO 10011 Dead - 19011 Is Released - A summary of differences
18. How to get my Auditor Certification
19. Rank of Findings
20. Auditor Development Plan
21. Auditing the Development function of my company - Strictly a Desk Audit?
22. ISO 19011 - Report on US TAG Standards Group Meetings
23. Unannounced Random Audits
24. Date in the VCAR
25. Identifying Continuous Improvement Opportunities
26. Auditing R&D for ISO9000
27. Indicators of effective QS
28. AIAG's TS16949 Auditor requirements and customer-specific requirements
29. ISO certification - consistency or quality??
30. Registered Quality Auditor
31. ISO 9001 Implementation in a Very Small Company
32. Too many different types of audit!!!
33. Systems Audit of Information Systems
34. Does the system audit have to be done to remain in compliance?
35. Process and Product Audit Checklist - Product realization, Effectiveness of process
36. Auditor Certification - IRCA
37. Does an Audit Schedule have to be a Controlled Document?
38. Product Audits - Is it a requirement to measure at least 3 parts?
39. Audit Schedule
40. QSA 4.17.6 - Internal Quality Audits - Effectiveness of the corrective actions
41. ISO-9000 Audit (1994 revision)
42. Additional Quality Systems
43. Type of audits
44. Element 4.10.2.3
45. Should Systems Effectiveness Be Audited?
46. All documentation need to be refenced to Quality System?
47. QS - Section II
48. Calibration Auditor - AIAG pertaining to ISO/IEC Guide 25 accreditation
49. ISO 9001 Lead Auditor Training - Is transition course required?
50. Integrating Audits - Is it worth it?
51. Can we be audited to the 'Notes' scattered throughout ISO9001?
52. TS 16949 Auditor certification
53. Audits Before Assesment
54. Seeking a TS-16949 Auditor's Check List
55. Auditor interpretation of PO data - PO submitted for outside calibration
56. Auditor Progression
57. Auditing effectivness
58. Relative Elements to Audit
59. Can someone explain why?
60. Auditor Certification - IRCA/RAB 5 day lead auditor course and exam - Bad Experience
61. TS-16949 Desk Audit
62. Auditing ISO9001:2000 and Differences between ISO 9001:1994 and ISO 9001:2000
63. Quality System Training for Managers and higher level employees
64. Desk top Audit - Anyone here with experience with Desk top Audits?
65. Self Direct Training
66. Risk Based Audits ocussing on those areas of identified risk
67. Objective evidence for covering all shifts and locations
68. Lead Auditor Requirements and Generating A Procedure For The Lead Auditor Training
69. Audit Teams - We have trouble keeping auditors
70. Question for ISO9000 auditor training
71. Auditing Management - Do I need to interview anyone in Executive Management?
72. Corrective actions - The act of having an MRB review and disposition
73. Audit Program
74. Interviews - What do Registrars really look for in an Auditor?
75. Auditor Procedure
76. Is ISO10011 Dead?
77. Audit Crisis - The entire management has left
78. Quality System development and implementation plan
79. Auditor Certification II - Auditor Certification - IRCA/RAB 5 day lead auditor course
80. Auditor Certification III - Auditor Certification - IRCA/RAB lead auditor cours
81. auditing and accounting
82. TS 16949 Certification
83. TS 16949 auditor registration scheme
84. Lead Auditor Course - Auditing to the ISO 9001:2000 Standard
85. When to start a formal corrective action as a follow-up action after audits
86. Career in ISO Auditing
87. Interpreting the Sanctioned Interpretations
88. Maintenance Audit Passed
89. Is a Newsletter Worth It?
90. Internal Quality Audit - Desk Top Audit First?
91. Registrar's Registration Audit Checklist
92. Observing an audit
93. Looking for an Auditor
94. Database of Auditors
95. iso 17025 registrars
96. Auditor Cartoon
97. What will the Auditor ask Top Management?
98. Audit Schedule Breakdown
99. ISO 9001 Certification - Registration Body Recommendations
100. I read/heard that the ISO Standard Language is English - What about audits
101. International 'Gov't' Type Certification Audit (a.k.a. - Supplier Audit)
102. Auditing
103. How Do I Get Started in the Auditing Field?
104. Contract Auditing for Registrar
105. ISO 9001:2000 Process Based Internal Quality Audit Plan
106. Auditing of Supply Department
107. ISO/FDIS 19011 (Español)
108. Software Supplier Risk Assessments
109. 3rd Party Audits and Clause 8.2.2
110. Internal Quality Audits and Contract Audits
111. Failures in Auditing and Auditing Companies
112. Audit Definition in ISO 9000:2000 includes "documented process"?
113. Ethics: Audit Question points auditor to a possible nonconformance
114. What to audit against clause 6.4 of ISO 9001:2000
115. Auditing Statistically - A statistical approach to sample sizes
116. Quality Auditor Certification vs. Lead Auditor Certification
117. Certified under 9001-2000 Globally/Internationally
118. Product Audit Scoring - Using a Point System for Product Audits
119. Available Auditors
120. Auditing 4.17
121. Electrical Engineering Group Audit Checklist
122. Quality in JAA
123. Quality Audit Report - Report Format and some Formal Sentences
124. Auditor Involvement in CA
125. Auditing - Best Practices
126. Auditing after a merge
127. Auditing 5.4.2 Quality System Planning
128. Roving Audits - Main functions is to audit the manufacturing process
129. Review Requested
130. Customer Audits and Guides
131. Auditing Human Resources and Daycare
132. ISO 19011 - Where can I find a copy?
133. Interesting audit request - Full reaudit when separating R&D from division
134. Quality Professionals as Executives
135. Evaluating 5.3 c - Quality Policy - Framework
136. Registrar Lead Auditor qualifications - What are the
137. Production Quality Tech Automotive
138. SAC - Semiconductor Assembly Council
139. Auditing 6.4 Work Environment
140. Pre-Audit Panic Mode - ISO9001
141. ISO 9001:2000 Auditor Transition Course
142. ISO 9000:2000 Transition Plan
143. ISO 9k2k 8.2.3
144. ISO 9001:2000 Audit Checklist Needed
145. Complete audit before assessment?
146. Process and system auditing - numerical score methods
147. ISO TS-16949 First Edition checklist
148. Auditing the Packing Dept. - What is the Packer Required to Have Available?
149. PO Requirement - Documents of external origin are identified and controlled
150. ISO 19011 (Quality and/or environmental management systems) has been published by ISO
151. What will ISO 19011 replace?
152. BSI-CEEM RAB approved ISO 9001:2000 Lead Auditor Course
153. 19011 Draft vs Final
154. Who - What is a Lead Auditor?
155. Audit issues help
156. I have a copy of ISO 19011. Do you have one?
157. External Auditing
158. Measurement system that has a Least Count of 1/10th of the tolerance
159. Not Aware of Department Objectives
160. Availability of Work Instructions for Standards Room Personnel
161. Qualifying audits
162. Data Center Audit
163. NQA Laboratory Services
164. Unorthodox auditing - Giving auditees a brief version the checklist before the audit
165. receiving materials
166. ISO/TS 16949:2002 Certification Body Auditors
167. Corrective actions
168. Segregation of Product by Type and Production Week - Warehouse
169. How can an individual become certified to be a QS 9000 or TS16949 Auditor?
170. Becoming lead auditor in ISO13485:2003
171. Effectiveness of a manufacturing process?
172. Audit based on guideline
173. Auditing to ISO 9001:2000 - What is the Process Model in PRACTICAL terms
174. Seeking: ISO 9001:2000 Audit Check List
175. Can I issue a NCR if the auditee did not comply what he is suppose to do?
176. Number Of Surveillance Audit Days For Remote Sites
177. Auditing Process and System to TS 16949 - SMMT Industry
178. TS 16949 - Feasibility Review, including Risk Anaylsis vs. FMEA
179. Classification of Findings in Audits to the new standard
180. ISO 9004 6.2.2.2 has listed "periodic refresher programs for people already trained"
181. Classification of Nonconformance - Project Extended without Contract Revision
182. 8.2.2 - Opinions please... Audit schedule based on importance and 'status'
183. Pharmaceutical GMP Auditiing
184. What are some of the findings found during your desk audit and how was it conducted?
185. Major vs. Minor vs. Opportunity for Improvement - Product as well as Office Processes
186. Any ISO 17025 Auditors Here?
187. Seeking Auditor Case Studies - ISO 14001
188. Auditor Training Materials
189. I'm looking for GCP Complicance Auditors in Massachusetts
190. Passing CQA Exam - Passed on first attempt? Second? A Poll
191. QMS Lead Assessor Training Organization Recommendations
192. Seeking: 21 CFR 820 Audit Checklist
193. New ASQ CQA (certified quality auditor) body of knowledge (BOK)
194. Audit Reports - Typed or Hand Written?
195. Your description of a natural born auditor?
196. The Ideal Auditee
197. Re: Training for ISO 9K2K
198. ISO 9001:2000 vs. GCP - (Good Clinical Practice - environment)
199. Why internally audit ISO clauses for ISO 9001:2000? (Small company)
200. Thoughts on Auditing - Seeking opinions regarding a couple of auditing points
201. Audit Readiness/Sillyness
202. What is ISO 19011? Has it superceded ISO 14010, 14011, 14012 & 10011?
203. Good lead auditor course criteria
204. Pre-assessment Audit Worries for a Newbie
205. Example of a Registrar's Registration Audit Schedule
206. ISO 9001:2000 (2008) Registrar Audits: What Questions are Being Asked?
207. ISO 9001 Registrar Audits: Failure Modes
208. Tier 2 Certification vs. Compliance Question
209. Four Audits in One Month
210. Minor Nonconformance turning into a Major - Systemic failure throught an organization
211. Statistical Sampling in QMS (Quality management System) Audits
212. Reasons for early termination of an audit?
213. ISO 9001 Audit - Bank Branch - Checklists & Guidelines
214. Production Scheduling
215. External auditor agenda
216. Scope of TS 16949 Audit - Is it possible to limit the areas?
217. Auditing the Task (Process) Elements - Visual Map Attached
218. Question about ISO 9001 Registrar Audit Checklist - No more checklists?
219. ISO 14001 Registrar Audits: Failure Modes
220. AS 9100 Registrar Audits: Failure Modes
221. What are the Shortcomings of ISO 19011?
222. What methods are you using to teach the process approach to auditors?
223. If I audit my Processes, Have I audited the Standard?
224. The 10 Essential ISO 9001:2000 Audit Questions
225. Confidentiality Audit - Confidential Infomation and related Documents Audit
226. ISO offers free-of-charge ISO 9001:2000 'auditing kit'
227. Major NC or Not - Procedure Not Implemented and Repetitive mistakes/failures
228. Can a registrar recommend with minor non-conformities closed before end of audit?
229. Auditing Product Realization - Advice on common oversights to look for?
230. Process-based auditing in 14001 - Seeking Reviews: Audit Schedule Content Feedback
231. Audit Matrix - ISO 9001:2000 clauses and some of the sub clauses
232. Observations vs. Preventive Actions discovered during Audits
233. An interesting audit coming up - First combined ISO 9001 / 14001 surveillance audit
234. Free ISO auditing kits from the ISO folks!
235. Who accompanies 'the Auditor'? Should Auditors be Escorted?
236. IAF Audit Mandays - 70 employee design office
237. Audit Sampling methods - Discovery Sampling Defined and Discussed
238. "LEAD AUDITOR" terminology - 3rd Party Auditors can't make up their minds
239. Looking for any kind of audit process and results for reference
240. TS 16949: 2002 Audit Failure Modes
241. Purging much of my auditing stuff - Auditing stuff for you!
242. Are 3rd party (ISO9001 Registrar) auditors allowed to provide "Recommendations" ?
243. Responsibility / Authority not Defined / Communicated - Clause 5.5.1 - NCR No: 4
244. NCR No: 1 - 8.2.1 - Customer perception was not been conducted
245. Gaining experience for RAB QALA Certification
246. Virtual Audit by Internet or Electronic Communication - Do you have any success?
247. How many mandays should the ISO9001 registration audit be?
248. TS 16949 - Para. 8.2.2.1 QMS Audit - How are you meeting this requirement?
249. Audit Check List for Safety Machinery - Conformity with OSHA 1910
250. Combined audit - ISO 9001 and ISO 13485 - Why Separate Audits?