Resources & Inspiration
Digitisation in pharma CQV: How does it help?
In the regulated pharma environment, “what is not documented is not done”. While many organisations in the pharma industry have been using paper to document
New in the Team: Edmus Goh, Engineer, No deviation
What drew you to the pharmaceutical industry? Ever since I was young, I have always been interested in the Math & Science field and have
The pillar document of C&Q in the pharma industry
Our previous blog posts talked about the skills needed to be a C&Q engineer and the 7 guides you should read. This blog talk about
The 7 guides to unlock a successful risk-based CQV project
Our previous post talked about the skills a CQV engineer needs. In this article, we will give you the CQV starter kit with 7 documents
GMP certification case study: Back in the State of Control
Suspension of a site’s GMP certification imposes substantial stress and impact on business, as well as the potential shortage of market supply. This case study
Deviation in the pharma industry: what it is and what to do when it occurs
Pharmaceutical quality is quintessential. Any departures from pharmaceutical quality are called deviations and can occur at any point during a process or product lifecycle. Deviations
FAT Protocol Development:
Option 2 – Using Test Case Library
Hi there. This is Joon, your trusted Kneat partner. Thank you very much for clicking into another instalment of my vlog where I’m continuing to
FAT Protocol Development:
Option 1 – Client imports Word document provided by vendor
Hi there! This is Joon from No deviation, your trusted Kneat partner. I’d like to share with you today, one of the many different methods that can
