Procedure Creation specifically for dimensional (caliper, micrometer, dti)

garyf2017

Involved In Discussions
#1
Hi, I'm about to create our own internal procedure,how do I approach a procedure specifically for dimensional (caliper, micrometer,dti) should I check the OEM or check the British Standards?

And would it be a general procedure for all, even though we're applying for range of up to 24inches for example?

TIA:)
 
Elsmar Forum Sponsor
B

BoardGuy

#2
I would not create a procedure on how to perform dimensional inspection and how to use a mic or caliper. This would be akin to creating a procedure on how to turn on a light when entering a dark room.

What I would do is obtain or create training materials on how to use inspection instruments (pin gages, mic, calipers, radius gages etc.) and proper measurement method. To answer your question if they should be SAE (Americas) or BSI (England) standards derived would depend on your work location.

I would recommend the following sources for training materials:

Equipment manufacturer
Key word search here on the cove
Professional organizations like ASQ.
 

garyf2017

Involved In Discussions
#3
Thanks BoardGuy,

We are going for an ISO Accreditation and it's our first time to create our own internal procedure, because we normally use British Standard alone.

We're required to show our own internal procedure and just use BS as a reference.
 
Thread starter Similar threads Forum Replies Date
A Management of change procedure for ISO 45001 Occupational Health & Safety Management Standards 3
L Product and process Deviation procedure Manufacturing and Related Processes 1
C IVD Metrological traceability without a reference measurement procedure General Measurement Device and Calibration Topics 11
M GP-12 procedure form and requirements Customer and Company Specific Requirements 1
R Procedure pack EU EU Medical Device Regulations 0
B Process / Procedure - Radiographic (X-Ray) Non-Film Document Control Systems, Procedures, Forms and Templates 0
M Procedure for vigilance system according to new MDR EU Medical Device Regulations 0
M Procedure for clinical evaluation according to new MDR EU Medical Device Regulations 1
S Production Work Order Procedure 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
E System&Procedure pack or accessory EU Medical Device Regulations 0
K Contract Manufacturer Do they need a complaint procedure? Medical Device and FDA Regulations and Standards News 8
E Design and Development file Procedure ISO 13485:2016 - Medical Device Quality Management Systems 0
B Procedure facility license in karnataka Manufacturing and Related Processes 3
S MDR - System and procedure pack article 22 and all sub processes that apply ISO 13485:2016 - Medical Device Quality Management Systems 0
P Software verification and validation procedure IEC 62304 - Medical Device Software Life Cycle Processes 6
B Procedure packs with non-medical devices EU Medical Device Regulations 1
K Need procedure for D&D inputs? ISO 13485:2016 - Medical Device Quality Management Systems 4
J Example of a defined procedure for carrying out Material Review Board (MRB) Manufacturing and Related Processes 0
A ISO 13485 procedure change and reflect to legacy manufacture items ISO 13485:2016 - Medical Device Quality Management Systems 2
S What should i choose for "testing procedure" characteristics? (N95) General Information Resources 0
S Critical characteristic on manufacturing operations test procedure Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
A SPC procedure / flow chart Statistical Analysis Tools, Techniques and SPC 2
J Action Not defined in procedure - NC - Incoming inspection AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
E Procedure ( SOP) for Device Master Record ( DMR ) and for Device History Record (DHR)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
shimonv Document Control Procedure Header Content Document Control Systems, Procedures, Forms and Templates 4
U Procedure pack components EU Medical Device Regulations 3
G Control Plan & PFMEA Review Procedure? FMEA and Control Plans 8
J Strategy for MDR Regulatory Compliance Procedure ISO 13485:2016 - Medical Device Quality Management Systems 4
A IVD in MDR procedure pack EU Medical Device Regulations 2
G RoHS Procedure REACH and RoHS Conversations 2
John Predmore Configuration Management as a process instead of a procedure AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
L How to add exemption or statement to control of document procedure? ISO 13485:2016 - Medical Device Quality Management Systems 5
A Design and development procedure for API Spec Q2 Oil and Gas Industry Standards and Regulations 6
W Using tailoring guidelines to tailor a QMS procedure ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Change management procedure when 7.3 is not applicable ISO 13485:2016 - Medical Device Quality Management Systems 5
L Sample Procedure from Contract Manufacturer Prospective ISO 14971 - Medical Device Risk Management 1
T Internal Nonconformance procedure thoughts (AS9100) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
Anonymous16-2 SOP (Standard Operating Procedure) Numbering Document Control Systems, Procedures, Forms and Templates 7
M UDI procedure/ report 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
DuncanGibbons Resources for aiding in procedure, work instruction and manufacturing plan development and management AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
S Article 22 Procedure Pack Labelling EU Medical Device Regulations 4
N EU MDR - Applicability Article 22 Systems and Procedure Packs CE Marking (Conformité Européene) / CB Scheme 4
M Example of statement for procedure pack MDR Article 22? Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 0
R Procedure, Frequency and Acceptance Criteria for Replicate, Recalibration, Before-After and Intermediate Checks ISO 17025 related Discussions 8
B FDA-Medical Device Reporting (MDR )procedure compliant with 21CFR section 803 US Food and Drug Administration (FDA) 0
M MDR - Is a formal GSPR Procedure required? EU Medical Device Regulations 21
Moncia Production Planning procedure ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
Q Tracking Procedure Revisions (Document Control) Document Control Systems, Procedures, Forms and Templates 9
L Purchasing procedure and workload ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
J Roles and accountabilities procedure? ISO 13485:2016 - Medical Device Quality Management Systems 9

Similar threads

Top Bottom