SBS - The best value in QMS software

Preservation of Product in Administrative Services

Stijloor

Stijloor

Staff member
Super Moderator
#11
#11
AndyN said:
MaryJames - I still think you should exclude it. If you can't see a way to address it, then that's a clue........There's very little in ISO 9001 that an effective organization isn't already doing, so if you don't 'see it' as applying, then it probably doesn't. (I didn't want to imply that you are 'blind' to the situation, either;))

I am intrigued that it's the admin org. that's going for certification - I wouldn't have thought the CB would allow that. Without giving too much away, what does the 'other part' of the organization?
Click to expand...
Look at this post: http://elsmar.com/Forums/showpost.php?p=190721&postcount=8
 
Free Trial of DISCUS Desktop
Elsmar Forum Sponsor
M

MaryJames

#12
#12
Hellloooo,
Welll if i exclude it then what about the other link that I posted. In health services its definitely not an exclusion. How can it be here then? I have a feeling i am missing something.
Please help even if I am being dumb at the moment:eek:.
Thanks in advance
 
Paul Simpson

Paul Simpson

Trusted Information Resource
#14
#14
MaryJames said:
Hellloooo,
Welll if i exclude it then what about the other link that I posted. In health services its definitely not an exclusion. How can it be here then? I have a feeling i am missing something.
Please help even if I am being dumb at the moment:eek:.
Thanks in advance
Click to expand...
MaryJames, The reason I haven't posted up to now is because I feel we are trying to put a sticking plaster on a gaping wound. I get the feeling this company you are working for is doing things all wrong.

Some of the principles you should have picked up from the Cove is that processes flow across the organization and exclusions are only applicable if the organization doesn't do them.

For your hospital / health practice you need to look at the whole organization rather than department by department to get any benefit from ISO and the process approach.

If we start from there we may be able to provide some help. :)
 
H

harry

Super Moderator
#15
#15
The danger of asking bits or parts of question here and there is that you may end up getting a wrong answer (overall) because answers depends on the actual situation or having a 'true picture'. As professionals, nobody want to be accused of giving a wrong advice.

To the original poster, I suggest you recollect your thoughts and review your overall intention and when you are ready, please repost it in detail so that you can get a better answer.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
S How do you determine a Constituent Part - Clause 7.5.5 Preservation of Product? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M What is "protection" as in section 7.5.5 "Preservation of product" ? IATF 16949 - Automotive Quality Systems Standard 7
M ISO 9001 - 7.5.5 - Meaning of Identification and how it helps Product Preservation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
N Clause 7.5.5 Preservation of Product in a Home-Care Company? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
R ISO 9001 Clause 7.5.5 Preservation of Product - Application to Software Products ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
A ISO 9001 Clause 7.5.5 Preservation of Product - Apply or exclude? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 23
N Note interpretation - Ensure that the preservation of the product has been consider ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
J Applicability of 7.5.5 Preservation of Product in a Service Industry like Insurance ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
C 7.5.5 Preservation of Product - Marking and Labeling AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
A Preservation of Product - Service Industry - AS9100 Clause 7.5.5 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
M How is 7.5.5 Preservation of Product applicable to Health Care Services? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
L Product Preservation - Measure of effectiveness IATF 16949 - Automotive Quality Systems Standard 12
M Element 7.5.5 - Preservation of Product - We ship the product FOB Point of Origin ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
L Preservation of Product ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
D Preservation of Electronic Data / Information Technology ISO 13485:2016 - Medical Device Quality Management Systems 5
M Informational US FDA final guidance – Utilizing Animal Studies to Evaluate Organ Preservation Devices Medical Device and FDA Regulations and Standards News 0
I IATF 8.5.1.5 Requirements c) provision of resources and d) packaging and preservation IATF 16949 - Automotive Quality Systems Standard 1
S Methods used for Preservation of Salmonella Food Safety - ISO 22000, HACCP (21 CFR 120) 5
D AS9100 section for Warehouse/Preservation of materials? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
D Material Handling, Storage & Preservation Procedure for Aerospace Mechanical Parts AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
B Engineering Consultancy - Clause 7.5.5 (Preservation) and 7.6 Equipments ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
J Basic template for Preservation, Storage and Handling Document Control Systems, Procedures, Forms and Templates 5
W Process inputs and outputs - Purchasing and Preservation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 20
H Medical device Product Registration Registrars and Notified Bodies 2
A Can a power Supply be an accessory to a medical device, if it is an 'off-the-shelf' product. IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
M Extension to shelf life of new product under MDR EU Medical Device Regulations 1
lanley liao Are there guidelines for application of all API monogrammal product? Oil and Gas Industry Standards and Regulations 2
S ISO 11137- Simulated product vs SIP Other Medical Device Related Standards 2
K "World Class Product" based QM. I need advice. Quality Management System (QMS) Manuals 14
R IATF 16949 Certification for new site with transferred product--what is the impact with CSR and scorecards? IATF 16949 - Automotive Quality Systems Standard 0
William55401 Distributed By Product - Best Practices for Configuration Management and Purchasing Controls ISO 13485:2016 - Medical Device Quality Management Systems 0
R Compatibility studies - combination product CE Marking (Conformité Européene) / CB Scheme 4
R Compatibility studies - Medicinal Product and Medical Device Other ISO and International Standards and European Regulations 0
J Marking "Distributed By" to product with distributors' reference-code EU Medical Device Regulations 3
dinaroxentool Selling a product in Both UK and EU after Brexit UK Medical Device Regulations 9
P EU MDR Translation of Product Name EU Medical Device Regulations 0
N Is this a single integral drug device combination product EU MDR CE Marking (Conformité Européene) / CB Scheme 1
V New Product Model CE Mark Certification under MDR EU Medical Device Regulations 0
Sidney Vianna Informational APQP4Wind - Advanced Product Quality Planning for the Wind Power Supply Chain APQP and PPAP 3
K 510k FDA review, will they accept Biocompatibility result generated using feasibility product lots? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
G Adopting old product - compliance with IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 9
S How long does it take to register a product with MHRA? UK Medical Device Regulations 4
D Classification of product for clinical trials EU Medical Device Regulations 14
N Adding unclassified product to the medical device registration US Food and Drug Administration (FDA) 1
B Internal Auditor Competency - Product Auditors Internal Auditing 9
T PFMEA and Control Plans on legacy product FMEA and Control Plans 5
P FDA Approved Product Contact Parts ISO 13485:2016 - Medical Device Quality Management Systems 6
S AS9120B - 8.5.2 Delivering Split Product AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
S Classification of a product according to MDR EU Medical Device Regulations 3
optomist1 Informational Training IMDS - Management of Product Chemical Regulatory Compliance RoHS, REACH, ELV, IMDS and Restricted Substances 2

Similar threads

Top Bottom