Full Material Disclosure and IPC-1752A

Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
R Full Scale for Pressure and Vacuum Gauge General Measurement Device and Calibration Topics 1
B How to exclude empty rows in full factorial design analysis? Using Minitab Software 0
S OEM full range calibrations vs Validation special test points Medical Device and FDA Regulations and Standards News 1
E Any sample of a full software life cycle IEC 62304 report ( any class )? IEC 62304 - Medical Device Software Life Cycle Processes 4
D Accurately measuring Full Thread Length Inspection, Prints (Drawings), Testing, Sampling and Related Topics 11
Q Full or Partial FAI? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
F Grand Avenue Software, Q-Pulse or Qualio - which for a full eQMS? Medical Information Technology, Medical Software and Health Informatics 1
V Process, component or full product re-qualification: leaded to unleaded solder Qualification and Validation (including 21 CFR Part 11) 8
A When there is a 2 year lapse in production, is a full FAI required? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
K Implant Card - Full Manufacturer's Address - Space issues EU Medical Device Regulations 4
A ISO 9001 lead auditor as Full time career India Career and Occupation Discussions 2
Sidney Vianna ANSI acquires full ownership of ANAB - December 2018 ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 0
P AS9102 full FAl or a partial FAI after production inactivity period AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
L Is writing out the ISO9001:2015 standard full name a requirement ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 37
Tagin Does ISO 9001:2015 require a full internal audit annually? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 21
M Bringing blending in-house - Verification or full validation? (Disinfectants) ISO 13485:2016 - Medical Device Quality Management Systems 3
R ISO 13485:2016 Registration - NC on full cycle of internal audits ISO 13485:2016 - Medical Device Quality Management Systems 7
H Do you have to perform an full internal prior to IATF 16949 audit? IATF 16949 - Automotive Quality Systems Standard 21
C Full QMS Audit and Internal Audit Question ISO 13485:2016 - Medical Device Quality Management Systems 16
F MDSAP vs "Full" FDA Requirements? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
J Malaysia - Full Labelling Local Language Translation Other Medical Device Regulations World-Wide 1
Marc How did you "get" a full-time job? (A 2017 discussion) Career and Occupation Discussions 11
J Use of Harmonised Standards (Full or Partial) ISO 13485:2016 - Medical Device Quality Management Systems 1
O AS9100 AQMS AEA Qualification Audits 4 Full QMS AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
S OBL (Own Brand Labeling) - Full Quality to Production Quality EU Medical Device Regulations 5
S IEC 60601-2-27: What does "linear within ±20% of the full scale output" mean? IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
S When to switch from a Partial AS9102 back to a Full AS9102 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
Y Is CFDA registration required if the full system is registered by our distributors? China Medical Device Regulations 2
V General Full Factorial - Optimal Design Six Sigma 2
O Is a full Internal Audit cycle every year required? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
K Half-Fractional vs. Full Factorial Central Composite Design Using Minitab Software 6
K Experiments Using Full Factorial Design Using Minitab Software 12
T Inspecting Full Thread Depth with a Plug Gage Inspection, Prints (Drawings), Testing, Sampling and Related Topics 4
E Full Quality Assurance Certificate EU Medical Device Regulations 5
Marc Naked-image full-body scanners to be taken out of U.S. airports Travel - Hotels, Motels, Planes and Trains 14
R Full Time Internal Auditor - Where should I be looking for someone? Career and Occupation Discussions 15
P Help Setting Up and Analyzing 3 Factor 2 Level Full Factorial Design for DOE Using Minitab Software 3
M ISO/TS 16949 Clause 8.1: Full of Repetitive Requirements? IATF 16949 - Automotive Quality Systems Standard 1
K What does Data Logger Accuracy = ? 0.25% of Full scale ? 1 Digit Mean? General Measurement Device and Calibration Topics 4
S Cool Minitab Document 'Sample' - Help with FULL Version location/access? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
D Conductivity Meter Specification - What Is Accuracy +/- 1% Full Scale + 1 digit General Measurement Device and Calibration Topics 15
V Can I get Full PPAP approval when some components are at interim approval? APQP and PPAP 12
K Audit NC - No evidence of a full 5 Why Analysis for the Customer Complaint Problem Solving, Root Cause Fault and Failure Analysis 8
R How to understand the "full scale peak-to-valley output" mentioned in IEC 60601-2-27 IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
R What is the Full-form of API & FDF? Pharma Related Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
M Limited Calibrations - An instrument that will not pass a full calibration, OOT General Measurement Device and Calibration Topics 8
Q Full Job Description and Responsibilities in ISO 9000? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
B Samples for Customer Evaluation prior to Full Release 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 7
P Measurement Error Requirements - 99% or 99.73% spread to represent the 'full' spread? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
R CNC OTS Software Validation Separate from full IQ/OQ/PQ for 21CFR Part 820 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 9

Similar threads

Top Bottom