The key changes in new ISO 9001 are the requirement for determining context of the organization and addressing risks and opportunities and of course there are some changes in every clause of the standard.
Where do i start.
1. I know i am supposed to have a quality policy
2.The company mainly consults on EIAs, so correct me if i am wrong, i am supposed to understand the stages of the EIA process. I should have a project plan for the implementation of quality systems in this process from the Basic Assessment Report, Environmental Impact Report, Scoping report e tc. I should document the procedures for work done at each level
3.If it was OHSAS or ISO 14001, i know i would do a risk assessment or impact /aspect register, but in this case, not sure what i would do there.Do a risk register for poor quality documentation and the control measure to ensure quality products and services?. Where can i get templates for the risk assessemnt
4.Have checklists for documents that need to be produced by the company for the client,
5. An organogram , that would include the clients being sevices, not sure i know zve safety file and contents of safety file.
6.Would need to ensure quality in terms of administrative documents : of invoices, employees IDs, filing of all work being done for the different projects, both in soft copy and hard copy in a systematic way for tracing records
What have i left out, do u have anything else that i could use. and templates for documentation that i need to do
Answer:
The best way to start is to conduct GAP analysis to determine to what extent the company is already compliant with the standard and what needs to be done to achieve the full compliance with ISO 9001:2015, here is the link to our free GAP Analysis Tool https://advisera.com/9001academy/iso-9001-gap-analysis-tool/ Once you determine this you can develop a project plan for the implementation and define deadlines, responsibilities, resources, etc.
2. Yes, you need to identify all the processes inside the company and determine how they relate to the requirements of the standard and what needs to be done to ensure that the processes are compliant with the standard. There is no specific requirement to document every process in the company but it is very common since it helps with achieving compliance with the requirements for each process.
3. Requirements to address risks and opportunities in ISO 9001 is very different from ISO 14001 and OHSAS 18001, ISO 9001 does not require methodology or written procedure and it doesn't require any records to be made and the scope of the assessment is completely different, for more information, see this article Methodology for ISO 9001 Risk Analysis https://advisera.com/9001academy/blog/2015/09/01/methodology-for-iso-9001-risk-analysis/
I think you should go for both - ISO 27005 training will give you specific knowledge for information security risk management, while ISO 31000 will give you a broad knowledge on how to manage any type of risk in an organization, without providing you detailed methodology for particular types of risks.
By the way, the questions in this methodology are adapted for smaller and mid-sized companies.
Difference between List of Interested Parties and Conformance Evaluation Record
Answer:
The Appendix 1 List of Interested Parties is used for identification of interested parties and defining their needs and expectations, the Appendix 2 Conformance Evaluation Record is used for evaluation of conformance to the requirements of the relevant interested parties.
New ISO 9001:2015 and TS 16949
Answer:
ISO 9001 and TS 16949 are separate standards although TS 16949 has derived from ISO 9001. The decision whether to comply with ISO 9001 or TS 16949 or with both should be made on the top level of the organization. If your customers require only TS 16949 than you should go only with it, but the TS 16949 will also go through change as ISO 9001 so it will be easier to make transition of TS 16949 if you already made transition for ISO 9001.
Controls for IT department
Answer:
I am not sure if I have understood what you need, but if your IT department is interested in a code of best practices, can be interesting for them ISO 27002. In ISO 27001 you can only see in the Annex A a brief description of 114 controls, but in the ISO 27002 you can find a guideline about how to implement each control.
Controls that are more related to IT, and from my point of view, that can be important for your IT department are: A.9 Access control, A.10 Cryptography, A.12 Operations security, A.13 Communications security, A.14 System acquisition, development and maintenance, and A.17 Information security aspects of business continuity management.
By the way, remember that with the implementation of ISO 27001, you need to identify risks and reduced them, and for this, you only need to select the controls that can help you to reduce these risks.
Finally, our online course can be also interesting for you because we talk with more details about the ISO 27001 and the controls of the Annex A “ISO 27001:2013 Foundations Course” : https://advisera.com/training/iso-27001-foundations-course/
ISO 27001 and ISO 22301
2. Is there any blog where I can read detailed domains, controls for ISO 22301?
3. I wish to have a copy of ISO 22301... Is this something I will need to buy from ISO - Do you have any spread sheet which list all controls and you could share with me please.
The process is very similar as with other assets - you have to assess the risks related to the network and find appropriate controls. Some of the controls you might apply yourself, and some controls you might outsource to a supplier - this is what you have to state in Statement of Applicability. Make sure you specify all the obligations of this supplier in the agreement.