Author: Governance Docs

A practical GDPR implementation plan in ten steps: records of processing, lawful basis, DPIAs, data subject rights and…

A practical ISO 13485 implementation plan in ten steps, with realistic timings, what QMSR changed for US manufacturers,…

A practical ISO 27001 implementation plan in ten steps for the 2022 edition, with realistic timings and the…

IVDR classification decides whether a notified body is involved at all, which conformity route applies, and which transitional…

IVDR performance evaluation has no medical device equivalent to borrow from. Article 56 requires three separate demonstrations, Annex…

The IVDR transition deadlines everyone can name — 31 December 2027, 2028 and 2029 — are the least…

Most guides to the EU IVDR are medical device guides with the words changed. This guide covers what…

How to run an ISO 9001 gap analysis before certification: what to score, how to weight the gaps…

A practical ISO 9001 implementation plan in ten steps, with realistic timings, and the three steps quality projects…

The ISO 9001 procedures and forms a working quality management system contains, clause by clause — including the…

What ISO 9001 design and development templates must capture under clause 8.3 — planning, inputs, controls, outputs and…

What an ISO 9001 change management template must contain to satisfy clause 6.3 and change control in clause…