Free Whitepaper: Checklist of Mandatory Documentation Required by ISO 9001:2015
It is easy to become overwhelmed with documentation in the belief that every single process that is in place in an organization must be documented, without realizing that this is not necessary to meet the requirements of the ISO 9001 standard. The 2015 revision of the standard become more liberal regarding documentation requirements, meaning that […]
Free Whitepaper: Checklist of Mandatory Documentation Required by ISO 13485:2016
The latest version of ISO 13485 was published in 2016, which means medical device companies need to transition from the previous version of the standard and comply with the new requirements. One of the most important steps in the transition process, as well as in the initial implementation, is determining what documents and records are […]
Free Whitepaper: Checklist of Mandatory Documentation Required by IATF 16949:2016
The latest version of IATF 16949 was published in 2016 and the transition from the previous version is ahead. One of the most important steps in the transition process, as well as in the initial implementation, is determining what documents and records are needed for an effective Quality Management System (QMS) based on IATF 16949. […]