SBS - The best value in QMS software

What is the status of the next version of ISO 14001?

Sidney Vianna

Post Responsibly
Staff member
Admin
#71
Then it is up to each member country to decide if the standard is suitable for its market. Then users get to decide whether it adds value to their organization, improves their environmental performance and is worth the cost of change.

Ultimately the market will decide whether or not the standard meets their specific needs.
What I sense in these sentences is the veiled threat by some national delegations that their respective countries might not adopt the upcoming revision of ISO 14001 as a national standard. While consensus does not imply universal agreement nor unanimity, it seems that some of the opposing views as the standard is shaping up are fierce, and emotion might trump reason.

As I said earlier, maybe the ISO TMB failed to understand it's own context and deploy a RBT when they decided to mandate the HLS to all future ISO MSS's.
 
Elsmar Forum Sponsor
R

Reg Morrison

#72
From http://www.lrqa.com/news/2015/ISO-14001-Significant-progress-made-in-Tokyo.aspx

The ISO Technical Committee, ISO/TC 207/WG 5, concluded their meeting in Tokyo on 7 February 2015 and has made significant progress towards the approval of the ISO 14001 Final Draft International Standard (FDIS).

As announced by ISO on 22 January 2015, ISO 14001 has progressed to Final Draft International Standard – the next stage in the ISO standard revision process – following approval of the latest draft by an impressive 92 % at the end of 2014.

LRQA System and Governance Manager, Steve Williams said of the meeting, “Over the course of the meeting, the committee successfully reviewed half of the comments which were submitted against the Draft International Standard (DIS). In addition to this, further work took place in relation to definitions within the standard and in relation to clause 4 – Context of the Organisation and clause 6 - Planning. Following this, changes were made which also reflect the comments which were submitted.”

The remaining comments will be reviewed at the next meeting of the committee which will take place in the UK in April.
 
Thread starter Similar threads Forum Replies Date
K Status of ISO 17025 (Next Revision, Which Committee does it?) ISO 17025 related Discussions 2
B Evolution in my own time? "Promoted" to Engineering Status - Goals for next Year. Career and Occupation Discussions 13
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

Similar threads

Top Bottom