The Experts in FDA and USDA Regulatory Matters
EAS Consulting Group is a leading provider of regulatory compliance solutions to industries regulated by FDA, USDA, and supporting agencies. Our team of consultants provide expert guidance for all of your regulatory requirements.
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Food
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Dietary Supplements
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Pharmaceuticals
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Medical Devices
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Tobacco
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Cosmetics
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Veterinary
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Cannabis
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Seminars
Transition from Computer System Validation (CSV) to Computer Software Assurance (CSA)
The life science industries, including pharmaceutical, medical device, biotechnology, biological, and tobacco and tobacco-related products continue to embrace new technology to improve delivery of quality products in compliance with FDA. In addition, we’ve seen a trend toward making use of cloud services, Software-as-a-Service (SaaS) solutions, and other technical innovations such as use of Artificial Intelligence (AI), Machine Learning (ML) and Large Language Models (LLMs), such as ChatGPT that have more recently begun to be used more heavily in life science companies.
Webinars
We appreciate your patience as we prepare something exciting for you, and we can't wait to share it soon.
On Demand Webinars
cGMP Responsibilities for Own Label Distributors and Brand Owners
This webinar will help you understand how to meet the requirements of an Own Label Distributor and comply with FDA regulations.
Latest News
FDA Publishes 2026 Foods Program Guidance Agenda: What Industry Should Know
FDA Outlines Foods Program Guidance Documents Under Development for 2026 The U.S. Food and Drug Administration has published its guidance documents under development list for the Human Foods Program...
Building Food Safety Culture When No One Is Watching
Food safety culture is, at its core, about manners in motion – the everyday behaviors and small choices that add up to a safe, consistent, and trustworthy operation – and it works best when expectations are modeled from the top and lived by everyone on the floor. It grows through repetition: the same good habits practiced shift after shift until they become second nature.
Drug and Device Corner 2026 January
Reminder that per the CARES Act of 2020, drug establishments are required to report NDC volumes annually. This applies to all facilities that manufacture, prepare, propagate, compound, or process...
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