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View Full Version : ISO 19011 and ALL Auditing Discussions


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  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 (Espaņol)
  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?