Are you prepared for a random FDA audit? The United States Food and Drug Administration often announces their plans to audit your company at the last minute. With only a few days’ notice, what should you do first to prepare for an FDA inspection? And what can you expect once the investigator arrives?
FDA QSR inspections don’t have to be as dramatic as they sound. Preparation, planning, and clear expectations will make your next FDA audit less stressful, and you might even pass with flying colors. This paper describes exactly what to expect from an FDA audit and how to prepare for the inspector's imminent arrival in a concise, at-a-glance checklist. What you will learn in this 8-page white paper:
We answer all of these questions and many more in this white paper.
我们的专家将详细解读2023年韩国食品药品安全部(MFDS)指导文件草案更新下韩国医疗器械注册监管要求、分类标准、韩国良好生产规范(KGMP)等相关要求,并将依据多年韩国本地注册经验提供注册案例分享。此外,您还将了解到制造商在面对MFDS监管时需要关注的核心要点,相关研讨会内容包括:
阅读更多自新欧盟医疗器械法规MDR (Medical Device Regulation 2017/745) 申请日期起,欧盟医疗器械监管当局就发布了一系列新文件及相关支持服务,旨在帮助医疗器械制造商适应新法规变更后的法规环境。 对此,作为在全球范围内经验丰富的医疗器械及IVD器械市场合
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