I'm happy to report that, even with the COVID pandemic, I am still able to present at conferences. This month I will be presenting at Compliance Training’s e-Compliance Conference to discuss ’21 CFR Part 11: New Approaches to Old Tasks in implementing Paperless Validation’, looking at how changes to technology and systems and even the COVID19 pandemic are influencing how the Pharmaceutical Industry is validating Computerised Systems.
We are a UK based Pharmaceutical Consultancy specialising in Data Integrity, Computerised System Validation and IT Quality Assurance services. TS CSV QA’s mission is to deliver pragmatic fit for purpose solutions to our clients to support technological implementation and innovation in the Pharmaceutical and Healthcare sectors. Founded by Trev Simmons, Trev is a Fellow of the Research Quality Association, and an active member of the association, and is currently Chair of the Digital Information Governance and Information Technology (DIGIT) Committee as well as the Cross-GxP Working Party on Data Integrity.