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 matter, and why robust, long-term document and data management strategies and implementation (from creation through to destruction) are critical to proving the validity and trustworthiness of scientific research.
Furthermore, the session demonstrates how adherence to GCP requirements in the conduct of clinical studies not only ensures patient safety, but also enhances regulatory compliance.
Throughout, you are introduced to the principles and practicalities of document and data integrity as well as requisite governance frameworks required to enhance document and data integrity. To finish, you’ll understand how you can embed it as routine good practice within your organisational culture.
You can watch the recording of the webinar by completing the form below.
13 Jul, 2021
Panel Discussion Recording: TMF Futures 2021, Good data in the age of digital transformation
24 Sep, 2021
Regulation EU 536/2014: A Records Manager and Archivist’s Perspective
02 Nov, 2021