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Profile: An interview with Karina Ruth Tabacinic on some fundamental concerns of medical translation - Volume 23, Issue

Medical translation has had a fundamental role in the history of scientific knowledge – ancient, past, and modern. It involves a larger array of working parts than is commonly brought to bear upon the study of other semantic activities. It calls…

The periodic safety update report and post market surveillance report under the new EU Medical Device Regulation - Volume 31, Issue

The new EU Medical Device Regulation 2017/745 (MDR) requires companies to provide a periodic safety update report (PSUR) and a post market surveillance report (PMSR). Creating these reports will strengthen the post market surveillance and vigilance…

EMWA social media team - Volume 23, Issue

As most of you already know, EMWA is currently using social media to interact with its members on a daily basis, to share information and promote discussions. Social media are not just sources of information but also ways of interacting with…

Getting Your Foot in the Door - Volume 25, Issue

Welcome to Getting Your Foot in the Door or GYFD for short, the latest addition to MEW’s regular sections. It all started at the EMWA 2015 autumn meeting in The Hague. Derek Ho met up with the EMWA Executive Committee (EC) to talk about his idea of…

Time to make it shorter: Plain English in our context - Volume 24, Issue

Plain English in medical and scientific writing is not one-size-fits-all, because audiences differ. Advice on writing plain English abounds. In 1946, George Orwell, best known as the author of 1984, formulated a much quoted, compact set of rules for…

Transition to the EU Clinical Trials Regulation: Trick or treat? - Volume 32, Issue

The etiquette in clinical trial research requires companies to respect rules and to be precise and accurate. The new EU Clinical Trials Regulation 536/2014 (EU CTR) pushes companies and health authorities one step further – to be more flexible and…

Regulatory Matters - Volume 26, Issue

Medical writers are often involved in the preparation of submission documents such as clinical overviews and clinical summaries. The submission of the application (or, in the case of drugs already approved, a variation or supplement) is an important…

Challenges of paediatric drug development and impact of paediatric legislation - Volume 21, Issue

Medical writers are increasingly involved in designing and documenting overall plans in paediatric drug development, e.g. EU PIPs (Paediatric Investigation Plans) and individual components, e.g. protocols and study reports. It is essential to…

EMWA News - Volume 25, Issue

Baby alarm in the Social Media Team! The future of EMWA’s social media team is secured as we are expecting three babies. Utmost efforts have been taken to ensure they are equally distributed across the Twitter, Facebook and LinkedIn teams.Seriously,…

Taming Microsoft Word® - Volume 23, Issue

The long, complex documents that medical writers often work with can place unusual demands on a word processing program. Microsoft Word® is a powerful program, but that does not mean using it properly is always easy or intuitive. Many problems…

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Scope

Medical Writing is a quarterly publication that aims to educate and inform medical writers in Europe and beyond. Each issue focuses on a specific theme, and all issues include feature articles and regular columns on topics relevant to the practice of medical writing. We welcome articles providing practical advice to medical writers; guidelines and reviews/summaries/updates of guidelines published elsewhere; original research; opinion pieces; interviews; and review articles.

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