Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements

Description

Data integrity is a fundamental requirement in Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) environments, ensuring the reliability, accuracy, and security of data throughout the product lifecycle. Regulatory agencies such as the FDA, EMA, and MHRA have intensified their focus on data integrity compliance, issuing guidance and enforcement actions against companies that fail to maintain trustworthy records. With the increasing use of electronic data systems and automation, organizations must implement robust controls to prevent data manipulation, unauthorized access, and compliance failures. This training provides participants with a thorough understanding of global regulatory expectations, practical strategies for maintaining data integrity, and insights into industry best practices to mitigate compliance risks.

This webinar, Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements, provides a comprehensive overview of data integrity principles, regulatory expectations, and compliance strategies in pharmaceutical and clinical environments. Participants will gain insights into…