DNV?s ISO 14001/RC 14001/RCMS ANAB accreditation has been successfully reinstated

A

Auditguyy

#1
DNV’s ISO 14001/RC 14001/RCMS ANAB accreditation has been successfully reinstated

Good news for DNV! There are always road blocks to try and prevent us from reaching our objectives, but hard work and diligence will always pay off.

[FONT=arial, helvetica, san-serif]"DNV’s ISO 14001/RC 14001/RCMS ANAB accreditation has been successfully reinstated as of February 2nd. We have worked diligently with the ANAB to resolve the issues in the best interest of our clients and within the accreditation body’s guidelines.[/FONT]
[FONT=arial, helvetica, san-serif]We value your business and apologize for any inconvenience this may have caused.[/FONT][FONT=arial, helvetica, san-serif]"[/FONT]
[FONT=arial, helvetica, san-serif]Best regards,[/FONT]
[FONT=arial, helvetica, san-serif]Richard Stolk - President[/FONT]
[FONT=arial, helvetica, san-serif]Det Norske Veritas Certification, Inc.[/FONT]
 
Last edited by a moderator:
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
N DNV issuing six year ISO 9001 certificates? Registrars and Notified Bodies 2
M ISO 50001 Certification News - DNV Sustainability, Green Initiatives and Ecology 2
O ISO 9000 in Russia - Seeking opinions of DNV - Noregian Det Norske Veritas Registrars and Notified Bodies 4
Q DNV IEC 64100 Manufacturing Evaluation - What to expect? Other ISO and International Standards and European Regulations 4
V UN body suspends the accreditation of Norway's DNV (for CDM) - Times of India Miscellaneous Environmental Standards and EMS Related Discussions 3
D DNV Standards for inspecting offshore containers and baskets Various Other Specifications, Standards, and related Requirements 5
R Identify Medical Device characterstics as Annex C of ISO 14971 Risk Management ISO 14971 - Medical Device Risk Management 2
A ISO 17021-1:2015 toolkit General Auditing Discussions 2
N ISO 19011:2018 - 5.4.2 "...audit program should engage in appropriate continual development..." Training - Internal, External, Online and Distance Learning 4
P ISO 13485:2016 MDSAP Certification Fee Survey ISO 13485:2016 - Medical Device Quality Management Systems 4
A ISO 14971 PFMEA Manufacturing Risk ISO 14971 - Medical Device Risk Management 2
C SOP Template needed for ISO 13485 6.3 Infrastructure ISO 13485:2016 - Medical Device Quality Management Systems 5
T ISO 13485 8.3 - Non-Conforming Materials - on-line rework or part of process? ISO 13485:2016 - Medical Device Quality Management Systems 11
T ISO 9001 8.5.2. - Identification and traceability to Identify Outputs - Services ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
T Outsourced process in ISO 45001 Occupational Health & Safety Management Standards 2
K Overall residual risk according to ISO 14971:2019 ISO 14971 - Medical Device Risk Management 5
M Gap analysis on ISO 14971:2019 with previous revision ISO 14971 - Medical Device Risk Management 2
T ISO 9001:2015 - Small Shop ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
T ISO 17025:2017 requirement 5.7.b. about maintenance the integrity of the management system ISO 17025 related Discussions 1
M ISO 9001:2015 case study sample ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Sample of Nonconformity report for ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
Q ISO 9001 8.5.1 - Control of production and service performance ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
B Do IFU designs have to be document controlled under ISO 13485? Document Control Systems, Procedures, Forms and Templates 2
H ISO 13485 - Separate Microbiology Audits ISO 13485:2016 - Medical Device Quality Management Systems 3
M Case study help as per ISO 9001: 2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
M Case study solution help required as per ISO 9001 : 2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
C Production and Post Production feedback - ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 4
B New ISO 14971:2019 Harm: unreasonable psychological stress, and cybersecurity ISO 14971 - Medical Device Risk Management 13
T ISO 13485 - 5.5.1 Responsibility and authority - Small Company Independence ISO 13485:2016 - Medical Device Quality Management Systems 13
A Refusal to discuss ISO 9001 obligations... what to do? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
A What does this sentence "this symbol shall be used in the orientation shown" mean in ISO 780:2015? Other Medical Device Related Standards 4
B Can we be ISO 9001 certified without a physical office? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
D Test summary report example for design validation wanted - ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 1
J Informational ISO 24971:2020 Released ISO 14971 - Medical Device Risk Management 0
S ISO 45001 and outsourcing the transporation of products Occupational Health & Safety Management Standards 3
S Documenting Design Verification Test Results (ISO 9001) Design and Development of Products and Processes 1
A Question on ISO 14001:2015 - Are annual audits required? ISO 14001:2015 Specific Discussions 8
N Which EN ISO 17664 version compliance to EU MDR? Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 3
Sidney Vianna Informational New edition of ISO 29001 released (June 2020) Oil and Gas Industry Standards and Regulations 0
R Who is the customer in the ISO/IEC 17025:2017? ISO 17025 related Discussions 1
T ISO 13485 - Process validation at critical suppliers ISO 13485:2016 - Medical Device Quality Management Systems 7
L Combining 3 ISO 9001 registrations into 1 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Risk Analysis Flow - Confusion between ISO 14971 and IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 8
C Compliance with ISO 17025 requirement 8.4.2 - Controls - Records recovery ISO 17025 related Discussions 4
N EN ISO 13640:2002 vs EN ISO 23640:2011 Other Medical Device Related Standards 1
O ISO 13485 vs. GMP - Comparison matrix wanted EU Medical Device Regulations 0
K ISO 15223-1 Do Not Reuse and Do Not Resterilize Other Medical Device Related Standards 5
A ISO 10002:2018 Checklist Needed (Complaints Handling) Customer Complaints 5
N Sampling Plan for Internal Audits - ISO 2859 or 3951 - Or Neither? Internal Auditing 6
O ISO 13485 - Is management review required before stage 1? ISO 13485:2016 - Medical Device Quality Management Systems 6
Similar threads


















































Top Bottom