Medical Writing EU Regulations My First Medical Writing

Volume 29, Issue 3 - EU Regulations

My First Medical Writing

Abstract

In this release of My First Medical Writing, I have the pleasure to share with you a great article written by aspiring medical writer Shirene Melissa Singh. With over 5 years of experience as a university educator and researcher, she is passionate about writing about infectious diseases, immunological concepts, global health perspectives, and applied research. In this article, Shirene shares not only her knowledge but also her views on the current COVID-19 pandemic, in a very thorough and engaging manner that leaves the reader with a lot of food for thought. It has been a pleasure working with Shirene on her first article in Medical Writing.

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Articles

Editorial
President's Message
EMWA News
The In Vitro Diagnosgtics Regulation and the role of medicals writers
Eudamed's delay and its impact on discolsure of clinical investigations under the EU MDR
Recent and upcoming regulatory changes in the European Region: Opportunitiess for medical writers
New documents required by the medical device regulation
Risk management plans in the EU: Managing safety concerns
Scientific advice procedures in the EU – an overview ofthe regulatory background
EU software regulations: The new normal or innovation stagnation?
The new PubMed – underestimated regulatory obstacles
Ethical challenges in acknowledging professional writing support
Publication management software for medical writers
Regulatory Matters
News from the EMA
Medical Devices
Medical Communications and Writing for Patients
Getting Your Foot in the Door
Lingua Franca and Beyond
My First Medical Writing
In the Bookstores
Good Writing Practice

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  • Amy Whereat (SpeaktheSpeech Consulting, Asnieres sur Seine, France)

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