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The Comprehensive Guide to RIMS Regulatory Management Software

Introduction to Regulatory Management in Highly Regulated Industries Regulatory compliance is the backbone of highly regulated industries such as pharmaceuticals, biotechnology, and medical dev…

Unlocking the Future of Regulatory Affairs: The Role of Automation and Artificial Intelligence

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In today’s fast-paced, highly regulated industries, companies are under constant pressure to meet strict compliance standards. For businesses operating in sectors like pharmaceuticals, medical dev…

How Automated Document Management Transforms Regulatory Submissions

In today’s fast-paced regulatory landscape, staying compliant while managing vast amounts of documentation can feel overwhelming. Automated document management is emerging as the game-changer for …

SaMD – USA and EU Approach Differences

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As per the FDA, the term Software as Medical Device (SaMD) is defined as “software intended to be used for one or more medical purposes that perform these purposes without being part of a hardware…

eIFU Requirements Under the EU MDR and Regulation 2021/2226

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What is an eIFU?   In general, an eIFU is defined as a non-paper version of the instructions for use. Currently, the definition of an eIFU is not the same in each market. In the EU, accordin…

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