AMS2750 rev F discussion

#1
Hello All. I am wondering if I am just having trouble locating early discussions or if we haven't gotten things started yet with the new discussion of implementation of AMS2750F. I am a QM of a heat treat facility and am also NADCAP registered for 12 years. I was present for some of the AMEC meetings when the specification was being rolled out and tried to gather as much information as I could. I am building a matrix of changes so I can finish the migration to rev F confidently. I was wondering if there is a thread already started for discussions about this endeavor or if this is the best place to discuss this. If this already exists somewhere, please point me in the right direction. Looking forward to discussions and offering / receiving help as needed. - Randy
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
S AMS2750 rev D - para 3.2.6.2 - "Signature of the calibration company representative" Various Other Specifications, Standards, and related Requirements 3
H Performing a TUS on a Furnace used at One Temperature - AMS2750-E AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 27
S Double Thermocouple - Two types, same sheath (AMS2750/Nadcap) Manufacturing and Related Processes 9
C Where can I get AMS2750 training? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
R TUS Sensors in AMS2750 Calibration Requirements Various Other Specifications, Standards, and related Requirements 12
K Who conducts Training in AMS2750 Pyrometry in INDIA Training - Internal, External, Online and Distance Learning 2
G Why has Nadcap made AMS2750 a requirement for paint/dri-lubes cure ovens? Various Other Specifications, Standards, and related Requirements 5
mike10 QMS Update - Rev. up or start over? Document Control Systems, Procedures, Forms and Templates 2
F MEDDEV 2.7/1 rev 4 and MDR - Definition of Description of Principles of operation EU Medical Device Regulations 4
E Can we still use MEDDEV 2.4/1 rev. 9 when classifying a medical device product under MDR? EU Medical Device Regulations 4
C AS9100 Rev D 8.1.1 & APQP - Operational risk management process AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
Nicole Desouza AS 9100 Rev D Gap Analysis AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
R AS9100 REV D gap analysis matrix AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
L I'm looking for Translation Procedure Guide MEDDEV 2.5/5 Rev.2 (NOT Rev.3) CE Marking (Conformité Européene) / CB Scheme 0
dgrainger Informational Additional Guidance Regarding the Vigilance System as outlined in MEDDEV 2.12-1 rev. 8 EU Medical Device Regulations 1
bryan willemot Documenting past problem history for fasteners for AS9100 Rev D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
M CEP requirements in MEDDEV 2.7/1, rev 4 and MDR - Are all MEDDEV requirements still applicable? EU Medical Device Regulations 7
K MEDDEV 2.4/1 rev. 9 Classification EU Medical Device Regulations 1
A Definition of "Sensitive Products" Clause 8.5.4 (c) in AS9100 Rev. D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
TheMightyWife Clinical Evaluation MEDDEV 2.7.1 Rev 4 demonstration of equivalence EU Medical Device Regulations 6
J CER - Literature search strategy and PMV data Timeline - MEDDEV 2.7.1/ Rev 4 CE Marking (Conformité Européene) / CB Scheme 2
Sidney Vianna Informational UTC ASQR Rev.11 has a mistake; certification of distributors to IATF 16949 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
M AS9100 Rev D and Pin Gages General Measurement Device and Calibration Topics 7
S Gap Analysis MDR req/MEDDEV 2.7.1 rev 4 EU Medical Device Regulations 3
S General Awareness Training for AS9100 Rev.D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
P How To Transition From AS9100c to AS9100 Rev. D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
C AS9100 rev D 8.5.1 c 2 - Defining the Machine in-process frequency per ANSI/ASQ Inspection, Prints (Drawings), Testing, Sampling and Related Topics 8
H CER - Equivalent Medical Devices Criteria - MDR/MEDDEV REV 4 CE Marking (Conformité Européene) / CB Scheme 9
G AS9101 Rev F - Worksheets for internal auditing AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
C Qualification of Evaluator - Clinical Evaluation Report MEDDEV 2.7.1 Rev 04 CE Marking (Conformité Européene) / CB Scheme 3
P AS9100 rev D Quality Manual wanted - 2017 Quality Management System (QMS) Manuals 4
A AS9100 Rev D - Procedure for Product Safety & Control of Counterfeit Part (Format) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
J AS9100 Rev. D - Question about 8.4.3 (k) - Supplier Certificates AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
M AS9100 Rev. D Transition Audit - Number of Audit Days AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
Q AS9100 Rev.D Transfer of Work - Procedure and form templates AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
J NADCAP NDT (specifically RT) - Checklist AC7114 Rev. K, section 8.1.3 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
A AS9100 Rev:D in Spanish - where can I find a Spanish version? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
Q Sample of the MEDDEV 2.7.1 rev 4 Clinical Evaluation Report wanted Document Control Systems, Procedures, Forms and Templates 15
oldqamanager How will you handle Clause 6.1 - Risks and Opportunities for AS9100 Rev. D Auditors? Risk Management Principles and Generic Guidelines 22
A AS9100 Rev D - List of Required Procedures Document Control Systems, Procedures, Forms and Templates 5
B AS9100 Rev D - Traceability of Consumables AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
K AS9100:2016 (Rev. D) Required Procedures AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 19
J AS9100 Rev D Quality Manual Rewritten - Feedback Appreciated Quality Management System (QMS) Manuals 13
K AS9100 Rev. D Transition - Internal Audits & Gap Analysis Requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 14
B AS9100 Rev D Quality Manual - How are you organizing? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
B AS9100 Rev D Sequence and Interactions of Processes - How in depth do I need to go? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
D Design and Development Procedure example and Template wanted - AS9100 Rev D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
R Qualification of Evaluator - Clinical Evaluation Report MEDDEV 2.7.1 Rev 04 Other Medical Device and Orthopedic Related Topics 1
O Guidance and/or assistance on Transition to AS9100 Rev D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
R Clinical Evaluation according to MEDDEV 2.7.1 (Rev 4) - seeking template ISO 13485:2016 - Medical Device Quality Management Systems 6

Similar threads

Top Bottom