In this blog we explore the benefits of implementing digital technology in healthcare to kickstart digital transformation in the NHS

From clinical trials to manufacturing agreements, the development of medical devices requires a large number of signatures and approvals.

In 2018 the HRA and MHRA confirmed their requirements for e-signatures and eConsent. Here, we look at CFR 21 Part 11 and QES and how both apply to the UK.

Docusign is committed to supporting healthcare organisations. Learn more about the 5 reasons to digitise NHS Trusts/ Clinical Commissioning Groups (CCG).