Status of OHSAS 18001 - Occupational Health and Safety

R

Roger Eastin

#1
#1
Does anyone know the status of the ISO Safety and Health standard? The name is ... let me see... uh, SH18000? or SA18000?
 
Free Trial of DISCUS Desktop
Elsmar Forum Sponsor
Randy

Randy

Super Moderator
#3
#3
It's starting to come into use by many organizations. CEEM, DNV and BSI offer training on it. I think DNV and BSI are doing registration too.

I've used it some (I'm an EHS guy by trade) and like it. If you take out the word "safety" and insert "environmental" you basically have ISO 14000. Both documents are structured the same.

You need both OHSAS 18000 and 18001.
 
R

Roger Eastin

#4
#4
Forum for ISO 18001 - Occupational Health and Safety

Marc - ya think it's too early to start a forum for ISO 18001? I see AIAG is starting a committee on this standard which could mean that Big 3 may move to make this mandatory (from a 3rd party standpoint) for their suppliers too. (It's great to be involved in the wonderful world of ever-spiraling standards!)
 
Randy

Randy

Super Moderator
#5
#5
The AIHA is formally involved in developing a Safety Standard right now that looks like it is based on BS8800 & OHSAS 18001.
 
D

David Mullins

#7
#7
ISO doesn't appear to have a technical committee looking at this subject.

From what I can recall the last time ISO looked at the subject, too many countries could foresee human rights problems associated with such a standard and discussion didn't get too far. Seems you couldn't certify sweat shops and rug makers with children chained to looms. But you can get them quality certified/registered!

------------------
 
F

Fire Girl

#8
#8
Funny you should mention...

I was actually going to put in a post about that myself. I couldn't remember the number of the new H&S standard. The only thing I was wondering about is each country likely has different labour laws, etc. How will this work? For quality, I mean there aren't really any 'laws' per se governing this. But health & safety for sure there are laws. My company is just starting to develop a H&S System (yes we are a little behind the times). But I'm thinking that perhaps if there was a third party (other than the Ministry of Labour) to answer to they might take it more seriously.

More info on this new standard would be appreciated.
 
R

Roger Eastin

#9
#9
I brought this subject up because some time ago, one of the Big 3 reps (Dan Reid?) talked about the effect of the cost of health & safety on the price of cars. In addition, in that same article, he talked about compliance to sort of health/safety standard in the future. When I saw the announcement by AIAG about a committee on health & safety, I thought the Big 3 was about to come down with an edict to comply with ISO 18001 or BS 8800 or whatever. That was why I thought a forum on this might be a good idea.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
N Initial Status Review - Certification to OHSAS 18001 Occupational Health & Safety Management Standards 4
R Getting harder to track the status of each one of the contracts Contract Review Process 0
S Changing revision status of a reviewed document Manufacturing and Related Processes 4
Q Project Tracker - Something that shows the status of each project Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 5
S PPAP Progress - Visual Status Board APQP and PPAP 0
M Status of Medical Device Regulations in UK Post-Brexit Other Medical Device Regulations World-Wide 10
F Is there such a thing as 'Critical supplier' status under the Dept. of Health (UK)? Medical Device and FDA Regulations and Standards News 2
M Informational TGA – Current status of breast implant products in Australia Medical Device and FDA Regulations and Standards News 0
D AS9100 Inspection records - Is there a requirement to have gauge ID and calibration status AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
JoshuaFroud The withdrawal of Lloyd’s Register MDD & IVDD Notified Body Status CE Marking (Conformité Européene) / CB Scheme 1
M Informational Medtech Europe presentation – – Industry Perspective on the Implementation Status of the MDR/IVDR Medical Device and FDA Regulations and Standards News 0
M Informational Medtech Europe – Open letter to the European Commission on the implementation and readiness status of the new Medical Device Regulation (MDR) Medical Device and FDA Regulations and Standards News 0
D The Status of ROHS for Medical Devices - April 2019 REACH and RoHS Conversations 3
R Visually impacting graphics for Nonconformance status metrics for Management Report Nonconformance and Corrective Action 5
S VW Special status condition IATF 16949 - Automotive Quality Systems Standard 3
Q What is the ISO 9001:2008 certificate status after 15 Sep 2018? Registrars and Notified Bodies 7
S Checking status of Medical device Other Medical Device and Orthopedic Related Topics 2
qualprod SAI Global Status as of July 2018 Registrars and Notified Bodies 2
S Status products when/if the QMS ceases to function? EU Medical Device Regulations 1
S Financial status of critical vendor IEC 27001 - Information Security Management Systems (ISMS) 7
H IS there any database for list of CE marked Medical devices and there current status EU Medical Device Regulations 8
Marc The Voynich Manuscript - Status as of January 2018 After Work and Weekend Discussion Topics 0
T Customer special status and initial IATF certification IATF 16949 - Automotive Quality Systems Standard 12
M Measurement Equipment - Identification of Calibration Status General Measurement Device and Calibration Topics 25
B Calibration Status of Gauges for Training Only ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
W Determining the Status and Importance of the Processes and Areas to be Audited Internal Auditing 7
T EASA TAG Block 11 Status/Work issue Quality Manager and Management Related Issues 1
Sidney Vianna First AS9100:2016 certificate issued, March 2017 - Status of Transition Sept. 2018 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 117
E Status of proposed changes to Medical Device Directive EU Medical Device Regulations 0
S ISO 9001 Audit Checklist - Red, Yellow and Green status Quality Manager and Management Related Issues 10
A Product status has changed from "tested" to "listed" in the EU Pharmacopoeia EU Medical Device Regulations 1
M Reagent Status Identification - 7.4.3 Verification of Purchased Product ISO 13485:2016 - Medical Device Quality Management Systems 6
P Need suggestion on Software or App for Tracking Quality Plan Status Software Quality Assurance 1
I Drawing standard (VDA) - Drawings in 3 different status VDA Standards - Germany's Automotive Standards 4
F Checking Gages In and Out and Verifying Calibration Status Calibration and Metrology Software and Hardware 8
R AS9100:2016 Rev. D - Status and Information - May 2014 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
S Suspension Status - Rules 4th Edition IATF 16949 - Automotive Quality Systems Standard 5
Pancho "IRS" Request for recertification of foreign status [SCAM] After Work and Weekend Discussion Topics 6
L Status of Certificate of Free Sale Transfer to MHRA - 1 April 2014 Other Medical Device and Orthopedic Related Topics 3
K 7.6 c) c) Have Identification in order to determine Calibration Status Calibration Frequency (Interval) 3
M Private Label CLIA Waived Status 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
K Revision Status Identified only in Sharepoint Document Control Systems, Procedures, Forms and Templates 2
R KPI Review Meetings never discusses previous meeting action plan status Quality Manager and Management Related Issues 5
Marc Current Status on TS 16969 Registration Restrictions IATF 16949 - Automotive Quality Systems Standard 3
G Medical Device Company US Importer/Distributer Status 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
B ISO 9001:2015 Draft - Status ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 151
L How to change the status of "Initial Importer" on the FURLS site US Food and Drug Administration (FDA) 1
S Understanding FDA rules regarding MDDS Status and Clinical Trials 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
B How many days after an interview should I follow up on the status of the interview? Career and Occupation Discussions 10
Buckyb AS9100C Clause 7.4.1 Appoved Supplier "Conditional" Status AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7

Similar threads

Top Bottom