A special Supermoon comes—but what causes it? 14 November 2016

Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
J 1.11 Preliminary Identification of Special Product and Process Characteristics APQP and PPAP 4
J EU MDR getting closer - Special offer for Elsmar members 10/2020 EU Medical Device Regulations 10
earl62 What is the best way to control special characteristics in Control plan? Is it Mandatory to have SPC for IATF 16949? IATF 16949 - Automotive Quality Systems Standard 7
Y What are different Special Inspection Level 1-4 and General spesification 1-3 ? AQL - Acceptable Quality Level 0
L Special Processes for SERVICES AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
K PSA Special characteristics Customer and Company Specific Requirements 0
Watchcat Advantages to pursuing a Special 510(k) instead of a Traditional 510(k) Other US Medical Device Regulations 5
qualprod Managing a "special" customer into the QMS? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
S Special 510(K) - Labeling change from Rx to OTC Other US Medical Device Regulations 11
M Special Controls and Class II Medical Devices Medical Device and FDA Regulations and Standards News 18
A ISO 10993-7:2008/ Amd.1:2019 - Classification of special populations Other Medical Device Related Standards 3
H SPC for special characteristics - CSR - Control of SC and CC Statistical Analysis Tools, Techniques and SPC 1
L Special Processes - Technical reason concerning torque - Anaerobic compounds Manufacturing and Related Processes 10
M Informational US FDA Final Guidance – Special Premarket Notification [510(k)] Pathway Medical Device and FDA Regulations and Standards News 0
F Replacement Bone Screws - Traditional 510(k) or Special 510(k)? Other US Medical Device Regulations 7
F Assignment of Special Characteristics to government regulations IATF 16949 - Automotive Quality Systems Standard 5
qualprod ISO 9001:2015 8.5.1 f - Scope with customer special process requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
J ISO 13485 - 7.5.2 cleanliness , 6.4.2 validation of special processes, and 6.4.2 contamination ability to be exempt? ISO 13485:2016 - Medical Device Quality Management Systems 5
L Injection Moulding Process (Special Process) Validation Food Safety - ISO 22000, HACCP (21 CFR 120) 2
S The key differences in 510k types - Traditional vs. Abbreviated vs. Special US Food and Drug Administration (FDA) 0
D I'm new in IMDS special using the IMDS application Manufacturing and Related Processes 8
S VW Special status condition IATF 16949 - Automotive Quality Systems Standard 3
K Letter to file vs Special 510 for additional accessory in orthopaedic kit Other US Medical Device Regulations 1
P Special 510(k) - Modified Medical Device Description Other US Medical Device Regulations 8
P V&V for Special 510k 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
F CQI-23 Special Process Molding - Controls IATF 16949 - Automotive Quality Systems Standard 7
B AS9100 - Are special process suppliers required to be NADCAP accredited? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 15
A Non-destructive testing methods are special processes? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 18
P Sanctioned Interpretations - IATF 16949 Cl. 8.3.3.3 Special characteristics IATF 16949 - Automotive Quality Systems Standard 3
E IATF 16949 Cl. 8.2.3.1.2 - Customer-designated special characteristics IATF 16949 - Automotive Quality Systems Standard 1
T Customer special status and initial IATF certification IATF 16949 - Automotive Quality Systems Standard 12
J NADCAP - Supplier Special Processes Certifications Manufacturing and Related Processes 1
N Special Vs Non-Special Processes Misc. Quality Assurance and Business Systems Related Topics 15
D Customer-Designated Special Characteristics vs. Special Characteristics IATF 16949 - Automotive Quality Systems Standard 2
S IATF 16949 Clause 8.3.3.3 - Documentation of all Special Characteristics in Drawings IATF 16949 - Automotive Quality Systems Standard 2
A Special Procedures for Non Aerospace Customers AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
M AS9110C Clause 8.5.1.2 Validation and Control of Special Processes for Repair Station AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
C AS9102 Form 2 Information - Special Processes - Plating AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
S Metal Radiographic and Ultrasonic Testing - Special Processes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
M Special Characteristic - IATF Definition IATF 16949 - Automotive Quality Systems Standard 4
W AS9100D Clause 8.5.1.2 Validation and Control of Special Processes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 37
I Special 510k Imported Legacy Blogs 0
J Are Product Special Characteristic(s) Mandatory? IATF 16949 - Automotive Quality Systems Standard 4
Crimpshrine13 PFMEA Scope - Oversized Special Characteristic FMEA and Control Plans 4
Q US FDA UDI Compliance Question - Class II (Special Controls) Other Medical Device and Orthopedic Related Topics 4
Q Special 510(k) or New Traditional - Currently Inactive Products Other US Medical Device Regulations 2
E Special 510(k) for software change Other US Medical Device Regulations 1
E 'Special' 510k as a Predicate Medical Device? Other US Medical Device Regulations 3
P Records for outsourced special processes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
B Submit a Special 510(k) or "Documentation by our own" 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5

Similar threads

Top Bottom