Blog
07 Dec, 2021
Our top 15 EU Regulation 536/2014 questions – Part 2
Following on from our first instalment of regulation 536/2014 questions, we bring you part two in which we delve into more intricate questions asked by CROs and…
02 Dec, 2021
Our top 15 EU Regulation 536/2014 questions – Part 1
EU Regulation 536/2014 is coming into effect at the end of January 2022. As we approach the date, we are seeing an increase in the number of…
25 Nov, 2021
Webinar Recording: A demo of Arkivum’s solution for pharma and life sciences (December 2021)
Arkivum were delighted to host this introduction and demo of our digital archiving and preservation solution. If you’re based within the fields of pharma and life sciences,…
25 Nov, 2021
Webinar Recording: Clinical data integrity
This webinar helps you to develop your understanding of data integrity within the life sciences and healthcare sectors. You’ll get to see why it is an important…
18 Nov, 2021
Understanding eTMF and GCP FDA data retention requirements
Who is the FDA? The Food and Drug Administration (FDA) is the US regulator responsible for protecting the public health by ensuring the safety, efficacy, and security…
11 Nov, 2021
3 simple ways to improve your QMS
A quality management system (QMS) is a collection of processes focused on meeting customer requirements and enhancing their satisfaction with your service or product. Implementing a QMS…
