Answer:
I understand that you want to know if a certain ISO certificate is credible or not. I advise you to look into the certificate that you want to check and identify the name of the accreditation body under which the certificate was issued. Then with that name you can follow the procedure mentioned in this article - How to know whether ISO 9001 certificate is valid? - https://advisera.com/9001academy/blog/2018/05/23/how-to-know-whether-iso-9001-certificate-is-valid/ - to see if the accreditation body is authorized by the International Accreditation Forum (IAF). If the accreditation body belongs to IAF and you have doubts about the certificate you should contact the accreditation body and explain your concerns.
The following materials will provide you more information about ISO 9001:
- [free course] ISO 9001:2015 Internal Auditor Course - https://advisera.com/training/iso-9001-internal-auditor-course/
- book - Discover ISO 9001: 2015 Through Practical Examples - https://advisera.com/books/discover-iso-9001-2015-through-practical-examples/
Compliance obligations
Answer:
ROHS or REACH compliance are ISO 14001 mandatory requirements. For example, ROHS does not allow the use of lead in the production of heat stabilizers used with PVC, any life-cycle impact assessment will identify a problem with the use of certain substances in production.
The following material will provide you information about compliance obligations:
Answer:
In clause 6.2.1C AS9100 Rev D is talking about any requirements that you have identified as relevant to your QMS. This could be a customer requirement for traceability or on time delivery which you need to improve, or it could be a legal requirement for your industry such as hazardous waste management of chemicals that needs to be implemented or improved. These identified requirements could turn into the following sample objectives:
XYZ Company will reduce errors in traceability from 5% to 2% in the next 6 months.
XYZ Company will improve on-time delivery form 95% to 98% in the next 9 months.
XYZ Company will increase the number of trained personnel for hazardous waste management from 3 to 6 in the next 6 months.
Remember, with the new standard these objectives now also need to have a plan created to accomplish them, so this will be your next step.
For a better understanding of all the requirements you can see this explanatory whitepaper: https://info.advisera.com/9100academy/free-download/clause-by-clause-explanation-of-as9100-rev-d
Top management involvemenr
Answer:
According to clause 5 of ISO 9001:2015 top managements needs to demonstate is engaged and performs quality management system activities.
Specifically the new standard expects from the top management to be involved in the following activities, which you could include in his SOP:
- The establishment of a quality policy and quality objectives compatible with the context and strategic direction of the organisation
- The integration of the QMS into the organisation’s business processes
- The availability of resources needed for the QMS
These are the main benefits of implementing ISO 14001 in your company:
1) Improve your image and credibility
2) Help you comply with legal requirements
3) Improvement in cost control reducing the number of environmental incidents that may occur
4) Higher rate of success when implementing changes
5) Enable quicker improvement of processes
6) Reduce employee turnover
Regarding the environmental impacts, here are some that you can consider for your type of business:
- Aspect: Carbon management from energy use of a building - Impact: Air Pollution; Resource Depletion; Habitat Destruction
- Aspect: Carbon manage ment from travelling - Impact: Air Pollution; Resource Depletion; Habitat Destruction
- Aspect: Water use - Impact: Water Pollution; Resource Depletion; Habitat Destruction
- Aspect: Wastes - Impact: Water Pollution; Resource Depletion; Habitat Destruction
In order to determine the environmental impacts of your organization you need to first identify the environmental aspects related to the processes of your EMS.
ISO 27001 does not prescribe how an organization should write its documents, so this decision is up to the organization, based on the results of risk assessment, legal requirements (e.g., contracts, regulations or laws the organization must comply with), or if Top Management decides this practice will be beneficial to the organization.
Section: 3.1 Chyptographic Measures
Question: At the beginning of this section the document talks about related documents. About the guideline for information classification and about contractual and legal needs. About the second one: by this do you mean the list of legal, official, contractual and other requirements? If yes do I have to add the document in section 2 (reference documents)?
Answer:
Yes, the referred document is the list of legal, official, contractual and other requirements. Regarding the second, you have to list this document, or the similar one you already use in your organization, in the list of referenced documents. If you don't have such a List, then list all the legislation and contracts related to the use of cryptography.
Included in the toolkit you bought you have access to a video tutorial that can help you fill in the risk assessment table, but broadly speaking you can use historical data from your company, or opinion of the personnel most involved with the assets you are assessing to valuate the consequence and likelihood of the risks.
Lo cierto es que en esta nueva versión de la norma ISO 9001:2015 ya no existe la obligatoriedad de crear procedimientos. La nueva ISO 9001 nos habla únicamente de información documentada que es necesaria mantener, esto correspondería a la política de calidad, los objetivos, el alcance y los criterios para la selección de los proveedores; y también menciona que debe ser retenida información documentada, que se refiere a lo que se entiende como registros. No obstante, la organización puede determinar la necesidad de crear una serie de procedimientos que le ayuden a facilitar la implementación y mantenimiento de la norma.