---
title: "GMP Auditing & COVID-19: The Complete Guide to Remote Auditing"
description: Learn everything you need to know to successfully plan and conduct a remote GMP audit in the era of COVID-19 and beyond.
image: https://www.thefdagroup.com/hubfs/fda-WP-GMPAuditingAndCOVID19-LIAd-01.jpg
---

| ![](https://www.thefdagroup.com/hubfs/fda-WP-GMPAuditingAndCOVID19-CoverWhite.jpg) | Get our free guide # GMP Auditing & COVID-19: A Guide to Remote Auditing & Workforce Recovery --- **Strategies and Expert Advice for Ensuring GMP Compliance Now and Later** Travel and work restrictions have made in-person quality audits difficult if not impossible to conduct. To avoid compounding delays due to canceled or deferred audits, life science firms are increasingly turning to remote or “virtual” audits to maintain their assurance activities until normal operations can resume. In this guide, you'll learn the challenges of remote auditing and strategies for overcoming them from an accomplished auditor with firsthand experience. This guide addresses each phase of the assessment process: planning, document review, process review, facility review, interviews, and closing meetings.  **About the Contributor** **Neal Siegel** is an independent Quality/Regulatory consultant (IVD/Med Device/Pharma) with 25+ years of experience and a particular interest quality statistics and understandable, practical application in instances of compliance shortcomings. He has extensive, successful experience from lab bench to C-suite and welcomes opportunities to mentor and teach sustainable skills for the industry. **Download the free guide and get everything you need to plan and execute a remote audit with ease 👇** [Get the free guide »](https://www.thefdagroup.com/gmp-auditing-covid-19-remote-auditing#) |
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