Webinars Focus on Strengthening FDA Compliance Through Data Integrity
New York, Wednesday, 5 November 2025.
Upcoming webinars will guide companies on enhancing data integrity and aligning with FDA regulations, presenting essential strategies for modernizing compliance in digital record management.
Enhancing Compliance Through Data Integrity
On November 5, 2025, several webinars were announced to focus on data integrity governance, emphasizing strategies for aligning with FDA regulations, particularly 21 CFR Part 11 and 820. These sessions are designed to equip companies with the necessary tools to enhance data integrity and ensure regulatory compliance in FDA-regulated industries. As digital record management becomes increasingly vital, these webinars present significant market opportunities for businesses seeking to modernize their compliance frameworks [1][2].
Key Topics and Industry Experts
The webinars will cover a range of topics, including principles of data process mapping, which is a powerful tool to identify data flow gaps, prevent integrity breaches, and prepare for regulatory audits. Additionally, the sessions will delve into FDA 483 and warning letter trends and explore tools and techniques for mapping data flows to mitigate compliance risks [1]. John E. Lincoln, Principal of J. E. Lincoln and Associates LLC, with over 36 years of experience in FDA-regulated industries, will be one of the key speakers sharing insights on these topics [1].
Addressing Market Needs
The growing reliance on digital systems in FDA-regulated industries highlights the need for robust data governance strategies. The webinars will address this need by discussing newer approaches in data governance that align with the latest regulatory expectations from the FDA. These sessions are particularly targeted at professionals across various sectors, including Quality Assurance Teams, IT and Data Governance Teams, and Regulatory Affairs Specialists [1][2].
Navigating Compliance Challenges
As companies face increasing pressure to comply with FDA regulations, these webinars offer practical guidance on maintaining control over data and quality systems in a digital, cloud-based environment. Key compliance challenges include ensuring the accuracy, completeness, and reliability of data across the product lifecycle and meeting the FDA’s 21 CFR Part 11 requirements for electronic records and signatures [3]. Meredith Crabtree, an expert with over 30 years of experience in regulated industries, will provide insights into implementing effective quality management systems [3].