Before the 760mph Hyperloop dream, there was the atmospheric railway

Marc

Fully vaccinated are you?
Leader

Attachments

  • atmospheric railroad car.jpg
    atmospheric railroad car.jpg
    152 KB · Views: 178

Ronen E

Problem Solver
Moderator
That's awesome! I never heard of the atmospheric railway before. The current version with the magnetic coupling actually sounds likely to be feasible.

When I read about John Rearden, Flight Rail Corp's spokesperson, I couldn't avoid thinking of Hank Rearden (from "Atlas Shrugged")...
 
Thread starter Similar threads Forum Replies Date
C Bacterial endotoxin before sterilization ISO 17025 related Discussions 0
S Summative Study before Phase 3? Human Factors and Ergonomics in Engineering 4
M Confusion about Pre-Sub meeting, agreement meeting and determination meeting before IDE US Medical Device Regulations 0
T What should be considered or asked to certified body auditors before selecting them for AS9100 Audit? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
D Adding a Processing site to scope, shipping before certification? IATF 16949 - Automotive Quality Systems Standard 2
L 3rd party audit issues - No audit agenda received a week before the audit Registrars and Notified Bodies 7
K Before-After Data Analysis Statistical Analysis Tools, Techniques and SPC 1
M UDI IVD - before submission? US Food and Drug Administration (FDA) 2
G Mfr. Process Validation BEFORE Design Transfer? Other Medical Device and Orthopedic Related Topics 1
G Process Validation Before/After Sterilization? Design and Development of Products and Processes 3
Ed Panek Make sure you hire competent QA RA Folks before making a "Medical Device." Coffee Break and Water Cooler Discussions 1
Z Steps to take before an MDSAP audit for Canada Canada Medical Device Regulations 3
A Should we assign the PRRC before the date of application of MDR (26 May 2021)? EU Medical Device Regulations 0
M Go Live With New ERP System before Recertification Audit General Auditing Discussions 6
M Sample record for verification performed by importers before placing a device on the market EU Medical Device Regulations 0
W Redacting Info Before Giving to Auditor ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
G How to ensure dimension of tapping hole before plating is correct? Manufacturing and Related Processes 2
R SaMD - Placing on the Market before DoA EU Medical Device Regulations 2
N Validating Software before getting approved as Class 2 device US Food and Drug Administration (FDA) 5
F Closing a finding before closing meeting General Auditing Discussions 25
F Internal Audit before Pre-Assessment ISO 17025 related Discussions 2
O ISO 13485 - Is management review required before stage 1? ISO 13485:2016 - Medical Device Quality Management Systems 6
O ISO13485 implementation - Are internal audits expected before stage 1 audit? Design and Development of Products and Processes 3
R Procedure, Frequency and Acceptance Criteria for Replicate, Recalibration, Before-After and Intermediate Checks ISO 17025 related Discussions 8
S MDR Delay - MDD design Change? (before new MDR DOA) EU Medical Device Regulations 8
N China - Start manufacturing before change approval? China Medical Device Regulations 3
P How far an operator can reach into a machine before it becomes an ergonomic problem CE Marking (Conformité Européene) / CB Scheme 5
M Contractor Requirements before hire Occupational Health & Safety Management Standards 3
C Design Transfer Review - Before or after PQ validation? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
DuncanGibbons Why is 8.4 post-delivery activities before 8.6 release of products and services in AS9100D? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
C Shipping Medical Devices to US before pre market clearance US Food and Drug Administration (FDA) 1
M New medical device on the market before MDR EU Medical Device Regulations 12
Q Release of the first batch of a cleared product before process validation 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
M Medical Device News Brexit - Withdrawal Agreement and Political Declaration laid before Parliament following political agreement. EU Medical Device Regulations 4
O Reinstating a disqualified supplier—questions to ask before making a decision Supplier Quality Assurance and other Supplier Issues 2
S Expiry date vs. Best Before Date - Reagents ISO 13485:2016 - Medical Device Quality Management Systems 9
E ISO 9001 certification of the new plant before start of production ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 18
Q Surveillance Audit of 2008 before Transition Audit to ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 20
WCHorn Rendering Scrap Unusable before Disposal (AS9100D, Section 8.7) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
S Requirement for Sterilization Validation completion before issuance of ISO cert ISO 13485:2016 - Medical Device Quality Management Systems 0
P Should Data be Normal before Computing Baselines? Statistical Analysis Tools, Techniques and SPC 4
L IEC/EN 60601-1 Certificate required before CE Marking? IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
P Is ISO 9001 Model tested for its effectiveness by ISO before its release? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
O Is it "legit" to create IMDS before Part Production? RoHS, REACH, ELV, IMDS and Restricted Substances 4
Crusader The calm before the storm... ISO 9001:2015 Registration Audit Coffee Break and Water Cooler Discussions 21
H Require PPAP Before Qualifying Vendor? (Packaging) APQP and PPAP 2
Q Is it normal practice to lubricate Ring Gages before use? General Measurement Device and Calibration Topics 17
chris1price Calibration of Instrument before being Discarded General Measurement Device and Calibration Topics 9
V Is 'Compliance' a pre-requisite or is it ok before Batch Release to Market? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
S Sell a Non-RoHS device, manufactured before RoHs regulations became effective? EU Medical Device Regulations 2

Similar threads

Top Bottom