Semiconductor Commodity Supplement 7.3.2s - Leadframe for semiconductors

C

cheahga

#1
Hi All,

After reviewing the semiconductors supplement of TS 16949 on the clauses 0f 7.3.2S, I'm a bit confused. What does this mean to us? Would you please enlighten us on this topic..... :frust:

7.3.2(d)S Design and development input
Device and process simulation model robustness shall be reviewed periodically to assure design and process compatibility. The organization shall have a documented procedure defining the review methods and frequency. This procedure shall include the extraction of key semiconductor parameters to verify process to model robustness.
NOTE: For semiconductor organizations, it is not required that CAD/CAE systems be capable of two way interface with customer systems unless this capability is requested by the customer for specific parts. When a new process or technology is being designed, the organization shall consider the customer product life cycle vs. the process or technology life cycle being developed. When a technology or process is identified as becoming obsolete, the organization shall notify the customer and develop plans
to manage the obsolescence. See also 7.3.7 S.


We are manufacturing leadframe for semiconductors and how will this affect us....

Hope to hear from anyone of you outthere.... :eek:

Many thanks in advance
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
Q Concerning Special Characteristics Interpretation - Semiconductor commodity standard IATF 16949 - Automotive Quality Systems Standard 3
K What are the current ISO/ TS 16949 Semiconductor Manufacturer Requirements IATF 16949 - Automotive Quality Systems Standard 12
L FMEA Rankings for Semiconductor Products FMEA and Control Plans 9
H How is a Semiconductor / Electronic Part Manufacturing APQP and PPAP 1
I Should chemical use within a semiconductor facility be an aspect? ISO 14001:2015 Specific Discussions 2
S Can enclosure of semiconductor or electrolytic capacitor provides basic insulation? IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
Q Semiconductor Inductor Failure - Will HAAS/HALT or any other test detect it? Manufacturing and Related Processes 4
R Semiconductor Reliability Testing for System - Operating Life Test Reliability Analysis - Predictions, Testing and Standards 11
A Cleanroom class in semiconductor Other ISO and International Standards and European Regulations 8
T Mil Std Certification for a Semiconductor Burn-In Process provider Various Other Specifications, Standards, and related Requirements 2
N ISO 9001 Implementation - Fabless Semiconductor (ASIC) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
Q Definition Excursion - Semiconductor, Definition for Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 4
Jen Kirley Cleanroom Standard for Semiconductor Fabrication Wanted Various Other Specifications, Standards, and related Requirements 3
R TS Certification Scope - Semiconductor subcontractor providing assembly and testing IATF 16949 - Automotive Quality Systems Standard 14
A Supplier Quality Management Strategies - Semiconductor Assembly and Test Services Supplier Quality Assurance and other Supplier Issues 6
antoine.dias What are the current automotive semiconductor requirements? IATF 16949 - Automotive Quality Systems Standard 2
K Predictive Quality Indicators - Manufacture of semiconductor optoelectronic products Quality Tools, Improvement and Analysis 2
D Should the clean room be called a laboratory? Semiconductor industry IATF 16949 - Automotive Quality Systems Standard 7
T Can a Fabless Semiconductor Company achieve TS16949 Certification (Registration)? IATF 16949 - Automotive Quality Systems Standard 48
Q Defunct SAC (Semiconductor Assembly Council) Standards Various Other Specifications, Standards, and related Requirements 11
Q FMEA for Inspection and Test required by TS 16949? Semiconductor Sector FMEA and Control Plans 6
D Is Wafer Probe (On Wafer Test) a Laboratory? Semiconductor Industry IATF 16949 - Automotive Quality Systems Standard 8
W ISO/TS16949 Certificate Withdrawn by CB - Burn-in services to semiconductor companies IATF 16949 - Automotive Quality Systems Standard 7
C Semiconductor Subcontractor Quality System Supplier Quality Assurance and other Supplier Issues 6
D Gage RR to train operators? QS-9000 Semiconductor Supplement 4.11.4.S Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 3
X Modeling and Analysis of Semiconductor Manufacturing (MASM) Conference Statistical Analysis Tools, Techniques and SPC 3
R Is Gage R&R with measurement data possible in a Semiconductor Fab? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
N TS16949 Quality manual for a fabless semiconductor company Quality Management System (QMS) Manuals 0
V TS 16949 Semiconductor Supplement Status - Obsolete? IATF 16949 - Automotive Quality Systems Standard 1
V Semiconductor Supplement to TS 16949 - Is the Semiconductor Supplement obsolete? ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 24
W Is the AIAG's Automotive Semiconductor Supplement Obsolete?? IATF 16949 - Automotive Quality Systems Standard 10
D First Pass Design Success - TS 16949 Semiconductor Supplement Design and Development of Products and Processes 5
Raffy SAC - Semiconductor Assembly Council General Auditing Discussions 1
J Looking for FMEA software for Semiconductor Industry Quality Assurance and Compliance Software Tools and Solutions 5
M Traceability - Semiconductor supplement QS-9000 - American Automotive Manufacturers Standard 14
W Semiconductor supplement General Auditing Discussions 4
O Supply chain strategy or commodity strategy reading recommendations Supplier Quality Assurance and other Supplier Issues 6
K Incoming (Receiving) Inspection for Commodity Items used in Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 11
Q ISO/TS-16949 Semi conductor commodity specification, the latest one dated 1/12/2004 IATF 16949 - Automotive Quality Systems Standard 3
B PMA Supplement Required? US Food and Drug Administration (FDA) 3
Anonymous16-2 Dietary Supplement Raw Material/Component Storage and Production Manufacturing and Related Processes 1
Ajit Basrur FDA News FDA Guidance Document: Manufacturing Site Change Supplement US Food and Drug Administration (FDA) 0
D FDA Registration - MD, OTC or Dietary Supplement US Food and Drug Administration (FDA) 0
Q 21 CFR Part 111 - Requirements for Dietary Supplement Manufacturing Water Quality Document Control Systems, Procedures, Forms and Templates 1
D DFARS (Defense Federal Acquisition Regulation Supplement) Raw Material Information Various Other Specifications, Standards, and related Requirements 1
Q Weighing Dietary Supplement Powder during manufacturing US Food and Drug Administration (FDA) 2
S Z299 Special Process Supplement Document Manufacturing and Related Processes 1
AnaMariaVR2 FDA GMP Inspectors Cite 70% of Dietary Supplement Firms Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
A Dietary Supplement Supplier Re-qualification Frequency and Criteria? Supplier Quality Assurance and other Supplier Issues 2
L Implementing ISO 9001: 2008 in a Dietary Supplement Company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1

Similar threads

Top Bottom