How to make a Product Requirement Document for a Transportation Company

E

elaurensia

#1
I work at shuttle company. I was assigned to make a product requirement document. How to make it? I have no idea... So, it comply with clause 5.4, 5.2, 7.2.1 ISO 9001:2008? Please help.:confused:

Thanks
 
Elsmar Forum Sponsor

John Broomfield

Leader
Super Moderator
#2
Re: How to make a Product Requirement Document for Transportation Company

elaurensia,

Product requirements document in your case is a specification for your shuttle service.

The relevant clause is 7.3 as the spec is output from your organization's design process.

You could develop this spec with your service design team and then document your service design process for your management system.

Or, you could capture the promise your organization makes to its shuttle service customers.

For further information google "service blueprinting".

John
 

Kronos147

Trusted Information Resource
#3
Interesting topic.

I would think to include On Time Delivery as a requirement.

Do you use shock sensors on the cargo? I would think maximum ranges should be specified if you do.

What other requirements can you determine? Fuel consumption?

Eric
 
E

elaurensia

#4
Hi John and Eric,

Thanks for your information, especially the google keyword.

Fuel consumption is also a good idea.

I've been putting together our promise to our shuttle customers.

I attached some of my ideas ... what do you think?

Thanks
 

Attachments

John Broomfield

Leader
Super Moderator
#5
Hi John and Eric,

Thanks for your information, especially the google keyword.

Fuel consumption is also a good idea.

I've been putting together our promise to our shuttle customers.

I attached some of my ideas ... what do you think?

Thanks
elaurensia,

Sorry, my Office365 subscription is not working at the moment because Microsoft has a problem with its cloud.

Would you please upload a PDF version of your Shuttle Service Promise.

Thanks,

John
 

John Broomfield

Leader
Super Moderator
#7
elaurensia,

I would add a section on the shuttle drivers.

Competent (includes drug-free)
Rested (includes records of time spent driving)
Retested for advanced driving skills
Etc...

Who makes sure the passengers are wearing their seat belts?

Would customers of other religions appreciate a prayer room?

Is there any need for a section on communicating with customers regarding timetables, pricing, cancelations, emergencies, etc?

John
 
Thread starter Similar threads Forum Replies Date
D Input Requirement Document for developing Product Presentation by Multimedia Solution Document Control Systems, Procedures, Forms and Templates 2
P REACH - A few of the hundreds components in my product no longer meet requirement REACH and RoHS Conversations 2
V Tell me about AS9015 Requirement for the delegation of Product Verification AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
E 7.1 (f) Question on this product realization requirement AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
D ISO/TS 16949 Requirement to 'Test Product in the Field' IATF 16949 - Automotive Quality Systems Standard 5
G ISO 13485 Requirement on labeling product in WIP (Work In Process) ISO 13485:2016 - Medical Device Quality Management Systems 4
C Requirement for NB audit with Discontinued Product EU Medical Device Regulations 3
A PPAP Sample Requirement - Using Product which has been Re-Worked APQP and PPAP 6
T Requirement for a Documented Process for the Review and Release of Product For Sale ISO 13485:2016 - Medical Device Quality Management Systems 6
G How to determine FDA Product Performance Requirement US Food and Drug Administration (FDA) 5
harrysons Automotive product transferring process what requirement to comply? IATF 16949 - Automotive Quality Systems Standard 3
V Product Design Skills - TS 16949 Clause 6.2.2.1 Requirement IATF 16949 - Automotive Quality Systems Standard 2
H TS 16949 Cl 7.2.2 - Review the Requirement Related to the Product IATF 16949 - Automotive Quality Systems Standard 1
P ISO/TS16949 MSA Requirement for Product Testing - Gloss and Grain Pattern IATF 16949 - Automotive Quality Systems Standard 3
M Customer Supplied Product and Traceability - No Customer Requirement - Toll Processor IATF 16949 - Automotive Quality Systems Standard 8
N Product Audits - Is it a requirement to measure at least 3 parts? General Auditing Discussions 4
S Art 117 product classification under rule 5 EU Medical Device Regulations 0
M Teeth Whitening Product Classification Canada Medical Device Regulations 0
M Safety assessment of cosmetic product EU Medical Device Regulations 1
H EMC & Safety Testing of the product with the same Sr. No. for EC Declaration CE Marking (Conformité Européene) / CB Scheme 3
P Product Requirements Control during Design Changes Design and Development of Products and Processes 3
D Digital Product Definitions Related Work Instructions AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
V Would the customer drawing change necessitate re-PPAP of the Product? APQP and PPAP 3
A Combination product Canada Medical Device Regulations 3
E UDI on product/packaging levels EU Medical Device Regulations 7
M Drug-Device Combination product CE Marking (Conformité Européene) / CB Scheme 1
H Product Safety & Conformity Representative (PSCR) Training Company IATF 16949 - Automotive Quality Systems Standard 0
X Design stage overview (Product specification) EU Medical Device Regulations 3
9 Responsibility for Product Paid for but not yet Shipped AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
M Product Acceptance Software (PAS) PROCEDURE (BOEING D6-51991) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
S Combo Product Assembly Process OQ Qualification and Validation (including 21 CFR Part 11) 0
V ADDING NEW MEDICAL DEVICE / Product, WHEATHER THIS AFFECTS EXISTING ISO 13485 CERTIFICATION? ISO 13485:2016 - Medical Device Quality Management Systems 4
A Product Liability Insurance coverage for EU Importer by UK Manufacturer EU Medical Device Regulations 2
sonflowerinwales Outgassing - product inside a sealed housing Manufacturing and Related Processes 1
L Temporary Product Deviation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
FRA 2 FDA Product NCRs- Quality Review Nonconformance and Corrective Action 6
armani 7.1.5 and design and development of product ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
M Aftermarket product PPAP approval IATF 16949 - Automotive Quality Systems Standard 1
G How to find applicable standards for a new product? EU Medical Device Regulations 6
T Link GMDN code and FDA product code US Medical Device Regulations 5
S Combination Product - Packaging US Food and Drug Administration (FDA) 6
S Can a product option change the product class? CE Marking (Conformité Européene) / CB Scheme 2
H Regarding EMC & Safety retesting requirements of the product CE Marking (Conformité Européene) / CB Scheme 2
Q Product audit assessment IATF 16949 - Automotive Quality Systems Standard 4
S Submit under a new product code in a 510k? US Medical Device Regulations 5
P Product Quality Review API-GMP Manufacturing and Related Processes 0
D Shelf life of non sterile class IIb product. ISO 13485:2016 - Medical Device Quality Management Systems 1
A Product Update and executing only affected System Tests, leaving out unaffected ones IEC 62304 - Medical Device Software Life Cycle Processes 5
K Can I make an exclusion of Design and Development in ISO 13485:2016 if my product is not regulated ISO 13485:2016 - Medical Device Quality Management Systems 12
M How to show the effect of the failure mode on the manufacturing process as a customer of product design process? FMEA and Control Plans 3

Similar threads

Top Bottom