A free weekly series for laboratory leaders on turning risk management from paperwork into daily control.
What you will learn
- Set up a risk process that meets current accreditation expectations
- Link incidents and near misses to risk entries and changed controls
- Spot the risks that paper compliance hides, such as interruptions and culture
- Show an assessor a clear trail from risk to action to verification
Who this series is for
Laboratory directors, quality managers, section heads and supervisors who need a working risk process before the next assessment. No prior reading is needed beyond working in or with a laboratory.
FormatShort written parts with one action to try each week
AccessFree to read on this blog, or by email
PaceOne part every Thursday
Parts
- ISO 15189:2022 after the deadline: what assessors check now Part 1 of 5
- CAP GEN.20315: how to build a prospective risk management process Part 2 of 5
Get this series by email
One short part a week for the length of the series, straight to your inbox. No other emails.