Any official doc/spec on different types of Yield calculation?

P

ProblemChild

Starting to get Involved
#1
#1
Where can I find an official document / standards that describe the many types of yield calculation to measure process performances?

Thanks
 
Elsmar Forum Sponsor
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
Howard Atkins Official TS answers from SMMT- Layout, System Audits, MR and Doc Control IATF 16949 - Automotive Quality Systems Standard 9
dgrainger Medical Device News MDR postponed - link to Official Journal of the European Union (24-4-2020) EU Medical Device Regulations 2
D Why does Official Journal list superseded standards? EU Medical Device Regulations 6
M Informational EU – Official position on EUDAMED delay Medical Device and FDA Regulations and Standards News 4
M Informational EU – Corrigenda for MDR and IVDR published in Official Journal Medical Device and FDA Regulations and Standards News 0
Q IVD vs EMC OJ (Official Journal of the European Union) Harmonised Standard Conflicts EU Medical Device Regulations 1
QMMike New Trend of not seeking Official ISO 9001 Registration ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 33
Q Compliance to EU Official Journal Harmonized Standards (MD/IVD products in EU) EU Medical Device Regulations 7
bio_subbu Official Journal of EU published two new RoHS Exemptions EU Medical Device Regulations 1
K May 16 2014 Official Journal of the European Union Publication - 60601-2-33 EU Medical Device Regulations 3
M Official EU Unique Device Identifier (UDI) Requirements EU Medical Device Regulations 3
T Official Language in EU required for Medical Device Labeling EU Medical Device Regulations 24
D Official Clarification of ECO, PDR, PCR Acronym Definitions ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
B Official Journal Postings Summaries for Medical Devices EU Medical Device Regulations 16
L Is there an Official Website for Medical Device Registration Information EU Medical Device Regulations 12
M Change Control - How low do you go before making official changes? Document Control Systems, Procedures, Forms and Templates 8
S AS9102 FAI for part number with no official drawing? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
K Are ISO 9001:2008 and AS9100:2009 going to be the official dates used? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
M Official Languages of the European Community ISO 13485:2016 - Medical Device Quality Management Systems 2
K New AS9101 - The Coordination Draft. Not the Official Release - IAQG9101 standard AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 76
D Official Government Regulatory Body Vigilance Contacts to use for China and for India ISO 13485:2016 - Medical Device Quality Management Systems 4
Manix Who is the Official Publisher of the APQP and Control Plan Manual? APQP and PPAP 2
SteelMaiden It's official, I am a quality geek Coffee Break and Water Cooler Discussions 3
A Definition Major Non-conformance and Non-conformance - Looking for official definitions Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 15
S EC Official Journal Harmonized Standards - Additional requirements? ISO 13485:2016 - Medical Device Quality Management Systems 3
CarolX Star Trek XI will begin filming this fall for Christmas 2008 release - It's official! Coffee Break and Water Cooler Discussions 10
Marc Intel-Macs owners now have an official second OS option - Windows XP After Work and Weekend Discussion Topics 10
S Is official MSA training required person performing calibration? IATF 16949 - Automotive Quality Systems Standard 6
Y Is there an official 6S Quality Management System? Is 5S being added to? Misc. Quality Assurance and Business Systems Related Topics 10
M 9K2K Training Method - Acceptable? E-mails as Official Training ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 15
Sidney Vianna Official ISO Interpretations - A Formal Process for ISO9001 Interpretation Requests ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 20
T How long until we get 'Official Paper' Certificate? Registrars and Notified Bodies 6
Howard Atkins QS-9000 Interpretations - July 2002 and the Official Announcement of the Death of QS QS-9000 - American Automotive Manufacturers Standard 9
E QS 9000 Official Web Site? QS-9000 - American Automotive Manufacturers Standard 5
D Naming of SOP doc's - Specific to Calibrations ISO 13485:2016 - Medical Device Quality Management Systems 2
K DoC (Declaration of Conformity) for Custom Made Medical Devices EU Medical Device Regulations 1
T Firmware version in EMC report / DoC CE Marking (Conformité Européene) / CB Scheme 1
T Single Point Contact / DoC CE Marking (Conformité Européene) / CB Scheme 2
Q Incomplete Process Sheets Closure - DHR - Doc Control Document Control Systems, Procedures, Forms and Templates 3
D Anyone Practicing Approval Signatures on Every Page of a Doc? ISO 13485:2016 - Medical Device Quality Management Systems 2
marmotte DoC (Declaration of Conformance) update required for Class II Medical Device? EU Medical Device Regulations 3
J Is there an ISO doc that is similar to DIN EN 10204? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
somashekar What comes first ... The DOC or the EC certificate from NB EU Medical Device Regulations 8
S Is there an Expiry Date for "Declaration of Conformity" (DOC) for Medical Devices? EU Medical Device Regulations 4
rob73 Harmonised Standards on DoC (Declaration of Conformity) EU Medical Device Regulations 10
rob73 Length of validity of a self certified Declaration of Conformity (DoC) for CE mark EU Medical Device Regulations 4
Q Japanese Pharmaceutical Affairs Law (PAL) doc and "Essential Principle Checklist" Japan Medical Device Regulations 2
J Using purchased "Training Doc" (TQS) software - Tips/Tricks Training - Internal, External, Online and Distance Learning 7
P Web based file sharing i.e. Dropbox for Doc Control - Comments/Alternatives? Document Control Systems, Procedures, Forms and Templates 6
S PMA Submission Software Hazard Analysis Document vs. Product Hazard Analysis doc ISO 14971 - Medical Device Risk Management 5

Similar threads

Top Bottom