Medical Writing EU Regulations President's Message

Volume 29, Issue 3 - EU Regulations

President's Message


What a busy time! The EMWA Professional Development Committee, the Conference Team, and the Executive  committee are working very hard on organising the virtual conference in November, which we hope will be a unique experience for you. The conference will start with an opening ceremony on Wednesday, November 4. On Thursday, November 5, we will have a variety of activities, including talks on predatory publishing, English sessions, how to work efficiently on your business, an exciting sponsored seminar, the freelance business forum, and the option to attend a mindfulness seminar. The symposium day on Friday, November 5, is about Research Integrity & The Medical Communicator: What We Do When No One Is Watching. The following 2 weeks will be packed with workshops. A big thanks to the workshop leaders who all made extra efforts to adapt their workshops for the virtual world!

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President's Message
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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