Approval of ISO 9001:2000 - Publication date as 15 December

#1
ISO has approved the Year 2000 revisions of the ISO 9000 series of
quality management standards and announced their publication date as 15
December. See the press release, "ISO 9000 revisions for publication on
15 December 2000"
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
K ISO 9001 Requirements for Raw Material Supplier Assessment and Approval ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
B Approval of Supplier with ISO 9001 (Automotive) General Auditing Discussions 18
W Internal Approval of Deviations - ISO 9001:2008 & ISO 13485:2003 Inspection, Prints (Drawings), Testing, Sampling and Related Topics 12
Q Does ISO 9001 Requirement for Document Approval (a service organization) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
W ISO 9001:2015 Clause 7.5.2 - Is Review and Approval applicable to Records? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 30
Q ISO 9001:2008 requirement for Design Organization Approval prior to "Repair" ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
T ISO 9001 Clause 7.4.1 Purchasing Process (Supplier Approval) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
L ISO 9001 Document Review and Approval Form Requirements Document Control Systems, Procedures, Forms and Templates 6
H ISO 9001:2000 Certificate - Original approval date 18 July 1995 and valid until 2012 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 27
B Requirement for Review and Re-Approval of Documents - ISO 9001 Clause 4.2.3 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
D ISO 9001 - Customer Approval of Design Changes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
S Document Control (Need an Approval Form) - ISO 9001 clause 4.2.3 Document Control Systems, Procedures, Forms and Templates 35
S Non-ISO 9001 Suppliers - Customer approval letters to use Supplier Quality Assurance and other Supplier Issues 20
J ISO 9001 and Type Approval certification Other ISO and International Standards and European Regulations 1
D Approval of FDIS ISO 9001:2000 - They've ordered a re-count - Too close to call ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
Q ISO 9001 2000 Drafts - What is the approval sequence and meeting places? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
R More on the approval of ISO 9001 : 2000 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
JoCam Difference between Approval and Registration - ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 2
R Concessions - ISO 13485:2016 requires concession approval from customers Nonconformance and Corrective Action 2
E ISO 13485 Clause 7.3.2 - Purchased Data Approval and Record Requirements ISO 13485:2016 - Medical Device Quality Management Systems 2
J ISO 17665-1 & 2 Review and approval of validation (of moist heat sterilizers) Other ISO and International Standards and European Regulations 3
T ISO 14001 Implementation Help & Question about Supplier Approval ISO 14001:2015 Specific Discussions 5
A Document Approval Requirements in an ISO 13485 and FDA System Document Control Systems, Procedures, Forms and Templates 7
M Impact of changing ISO 13485 registrar / notified body on Chinese SFDA approval ISO 13485:2016 - Medical Device Quality Management Systems 3
D ISO and IEC Certification for 510K Approval 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
J IRCA Approval of ISO/AS Courses - Need help ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 5
J Approval of Grandfathered Documents - ISO 9000:2000 Clauses 4.2.3 a&b Document Control Systems, Procedures, Forms and Templates 9
M Approval - FDA and ISO Definitions US Food and Drug Administration (FDA) 14
S Defining Document Review and Approval responsibilities - ISO 13485 - Medical Device Document Control Systems, Procedures, Forms and Templates 3
A Is ISO enough to satisfy these TQM approval questions? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
Marc Approval of ISO/IEC 17025 ISO 17025 related Discussions 2
B Document Approval Matrix Benchmarking Document Control Systems, Procedures, Forms and Templates 3
J Document Approval Signature Order Document Control Systems, Procedures, Forms and Templates 10
D Change Approval Requirements - Does every change need formal customer approval? Design and Development of Products and Processes 17
B SN95 Respirator Approval Information Other Medical Device Related Standards 0
P Notified Body Approval of Change EU Medical Device Regulations 2
Marcel DS GOST-R (Type approval for Vehicles in Russia) Other ISO and International Standards and European Regulations 0
K Joint approval between OEM and Manufacturer on Design Documents ISO 13485:2016 - Medical Device Quality Management Systems 4
O Radio modular approval in Brazil Other Medical Device Regulations World-Wide 2
O Radio Modular approval in China China Medical Device Regulations 0
dgrainger Clue to UK's new regulatory requirements - approval of all devices placed on the market? Other Medical Device Regulations World-Wide 1
was named killer AS9100 Supplier Approval Requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
F How to fill out an Appearance Approval Report (AAR) APQP and PPAP 0
Q Document approval through SharePoint (without signature) Records and Data - Quality, Legal and Other Evidence 4
U Document Approval - Software company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
M Production approval testing - Alternative ideas for Validation Reliability Analysis - Predictions, Testing and Standards 4
I Can a document (form) approval record be separate? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
F Medical Devices - Hong Kong - Post approval changes regulation (China's MOH) Other Medical Device Regulations World-Wide 3
F Medical Devices-South Africa _Post approval changes and Software Other Medical Device Regulations World-Wide 0
C NB approval - Basic question about Notified Bodies and their role EU Medical Device Regulations 10

Similar threads

Top Bottom