Excellent article in the Feb 2000 edition of Quality magazine on maintenance

R

Roger Eastin

#1
#1
There is an excellent article in the Feb 2000 edition of Quality magazine on maintenance. Although it is not strictly TPM, but it is an interesting approach to maintenance that has a lot of common sense in it.
 
Paper to QMS ad
Elsmar Forum Sponsor
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
J Excellent Resource on Statistics / Lean / Six Sigma Book, Video, Blog and Web Site Reviews and Recommendations 2
L Performance Excellent Plan in a Service Organization Service Industry Specific Topics 1
V Excellent references on Lean & Six Sigma ...from MIT Book, Video, Blog and Web Site Reviews and Recommendations 0
S What is the Secret of Excellent Quality in a Machine shop? Misc. Quality Assurance and Business Systems Related Topics 29
A Excellent Reference for MS Excel .xls files Excel .xls Spreadsheet Templates and Tools 9
P How to manage production? How to become an excellent production manager? Manufacturing and Related Processes 5
S What Constitutes an Excellent Quality Manual? Quality Management System (QMS) Manuals 18
Marc Root Cause Analysis and ISO 9001 - An excellent detailed discussion Problem Solving, Root Cause Fault and Failure Analysis 7
K Article 18: Implant Card and information to be communicated. EU Medical Device Regulations 5
R Requirements for MDR Article 22 Systems EU Medical Device Regulations 1
H MDD Article 12 Labeling for Class IIa Medical Device - Please Advise EU Medical Device Regulations 3
S Article 22 Procedure Pack Labelling EU Medical Device Regulations 4
N EU MDR - Applicability Article 22 Systems and Procedure Packs CE Marking (Conformité Européene) / CB Scheme 4
M Example of statement for procedure pack MDR Article 22? Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 0
S Translational Requirements - Article 120 EU Medical Device Regulations 5
S Class I MDR Article 10 – QMS EU Medical Device Regulations 1
K Expected lifetime of the device-Article 18 EU Medical Device Regulations 4
R Clinical evaluation without clinical data - MDR Article 61(10) EU Medical Device Regulations 6
A MDR Article 22 applicability - Legal manufacturer EU Medical Device Regulations 6
T Implant Card - Article 18.1(a) and MDCG 2019-8 clarification EU Medical Device Regulations 3
P Economic operator responsibilities - when the Importer is also Distributor - Article 13 EU Medical Device Regulations 1
M Medical Device Identification & Codes - Article 27 Requirements questions EU Medical Device Regulations 1
K Article 18 in the Implant Card - Expected lifetime of the device EU Medical Device Regulations 3
S Article 61 - MDR Clinical Investigation Requirement EU Medical Device Regulations 5
C Article 16 MDR - Medicine packaged together with Medical Device EU Medical Device Regulations 0
F MDR system/procedurepack (article 22) with device acc. to MDD and MDR CE Marking (Conformité Européene) / CB Scheme 2
T Sample of 1st Article Inspection Report wanted APQP and PPAP 3
N EUDAMED postponement and compliance with Article 120 (3) MDR for Legacy Devices EU Medical Device Regulations 8
R MDR Article 22: Systems and procedure packs Other Medical Device Regulations World-Wide 12
T EU MDR Article 61- Clinical Evaluation EU Medical Device Regulations 2
F 2017/745 Article 31 Single Registration Number Medical Device and FDA Regulations and Standards News 5
Sidney Vianna Interesting Discussion Interesting article form the UNIDO Magazine - CSR: a wolf in sheep’s clothing? Sustainability, Green Initiatives and Ecology 16
M Informational EU – Guidance document Implant Card relating to the application of Article 18 Regulation (EU) 2017/745 of the European Parliament and of the Council o Medical Device and FDA Regulations and Standards News 2
M Informational EU – MDCG 2019-7 Guidance on Article 15 of the Medical Device Regulation (MDR) and in vitro Diagnostic Device Regulation (IVDR) regarding a “person re Medical Device and FDA Regulations and Standards News 6
F Interpretation of MDR 2017/745 Article 23 - CE Mark Requirements EU Medical Device Regulations 8
A Interpretation of Article 16 (2b) - Packaging, samples and Certificate EU Medical Device Regulations 10
E MDR Article 117 / Impact to New Marketing Authorization Applications Other Medical Device Regulations World-Wide 1
G First Article Submission (Destruction of parts) APQP and PPAP 2
C Access to Technical Documentation - MDR Chapter VI Article 61 EU Medical Device Regulations 4
K First Article Inspection (FAI) - Equipment used - Dimensions vs. Go/No-Go ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M Informational MDCG 2019-3 Interpretation of Article 54(2)b – Pre- market clinical evaluation consultation procedure with the involvement of expert panels Medical Device and FDA Regulations and Standards News 0
T MDR article 22 - System of 2 CE products and validation / usability? EU Medical Device Regulations 10
C Is a First Article Inspection (FAI) Procedure required by ISO 13485? ISO 13485:2016 - Medical Device Quality Management Systems 3
M Informational MDCG 2019-2 Guidance on application of UDI rules to device-part of products referred to in Article 1(8), 1(9) and 1(10) of Regulation 745/2017 Medical Device and FDA Regulations and Standards News 0
K Article 23 (Parts and components) - Economic Operator EU Medical Device Regulations 1
Marc As the earliest wind farms age - Dec 2018 Ars article Sustainability, Green Initiatives and Ecology 4
T Clarification on MDR - Article 18(d) - Implant Card EU Medical Device Regulations 14
Sidney Vianna Interesting Discussion Article from Grant Ramaley in QD - MDSAP: When Is a Certificate Not a Certificate? Canada Medical Device Regulations 0
M FAI AS9102 - What does a First Article Inspection cover? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
C AS9100, Clause 8.5.1.3 - First Article Inspection Costs AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 16

Similar threads

Top Bottom