Audting: system and process audits

What is the difference between the system and the process audits? Can both be done at the same time? The answers in our new blog post: A system audit vs. a process audit

QMS Audit Frequencies

How often should the QMS processes be audited? What are the requirements and best practices?
QMS Questions answered: Audit frequencies

Control of nonconformities in ISO 9001:2015

Control of nonconformities documented information, object of control and other ISO 9001:2015 requirements changes in our new article Nonconformity Management.

How to evaluate Contract Review process effectiveness?

What factors can be used to measure the effectiveness of the Contract review process?
Is there a universal way to determine effectiveness in this process?
More on our blog Contract Review Metrics

New product: ISO/DIS 45001:2017 OH&S Manual Template

• OH&S Management system audit and certification
• Understanding of how the OH&S management system operates
• OH&S Personnel training

and more in our new OH&S Manual Template fully aligned with the new  ISO/DIS 45001:2017.

QMS Questions and Answers: ISO 9001:2015 clause 6.1

The first paragraph of ISO 9001 Clause 6.1 mentions clauses 4.1 and 4.2 - but this does NOT mean that actions to address risks and opportunities should be implemented in 2 phases:
Phase 1 Address Risk/Opportunity for Interested Parties and then Phase 2: Risk Assessment towards process.
The correct interpretation of this ISO clause in our blog Clause 6.1 Actions to address risks and opportunities QnA

Integrated Management System Pros and Cons

Some companies choose to integrate their processes into one IMS system. While others will build a separate ISO 9001 QMS, ISO 14001 EMS, etc.

Find out IMS Cons and Pros in our blog post Why should you prefer an Integrated management system (IMS) or not?