Course Overview
Understanding and incorporating Data Integrity and Data Quality (EMA Data Quality Framework for EU medicines regulation) into processes is crucial in the Life Sciences industry when it comes to GMP data.
This one day course aims to thoroughly examine the foundations of Data Integrity and Data Quality and integrate them into processes within regulatory frameworks. Practical examples of data integrity risk analysis evaluations conducted within regulatory frameworks will be covered in this session.
Join this course to learn how to apply and take advantage of Data Integrity and Data Quality.
Benefits of attending:
Who should attend?
This course is ideal for Business Process Owners and Validation managers.
It will be relevant for everyone who participates in validation and compliance activities, both on managerial as well as on expert level, particularly those working in: