Pharma: Clinical data

Data integrity is a critical issue in document governance and is increasingly becoming a focus for regulatory inspections globally. This course will equip you with the necessary knowledge to identify and avoid potential data integrity issues before auditors do.

This workshop will focus on the effective use of metrics to monitor the real progress of your clinical research project. A valuable master class for anyone involved in clinical research.

This course will assure monitors understand the importance of compliance with latest ICH GCP R3 requirements, and how these apply to monitoring clinical trials in the future.

During this course, data integrity will be discussed from the perspective of GxP audits, with practical advice for successful data integrity audits given.

Explore how human behaviour and stakeholder dynamics create hidden risks in clinical trials. Using the CURED framework and interactive learning, participants will learn to identify and manage relational risks that undermine trust and collaboration. The result: stronger teams, better communication, and more resilient project outcomes.