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This week, less is more

First, we go local, with two announcements from the European Medicines Agency (EMA). Then, an article about the micro level checks on which existing molecules can be repurposed to treat SARS-CoV-2. Lastly, a Science article reveals that excipients (drug...

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New to medical devices? Here are 3 insights about Clinical Evaluation Reports

After completing a three-module course about how to write a Clinical Evaluation Report (CER) from the new Medical Device Regulation perspective, I realised there were many things about the topic that I thought I knew but I didn’t. I’m going to share some of them with you, hoping that they’re useful if you want to specialise in writing for medical devices.

Who runs the blog?

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Diana Ribeiro is a pharmacist and freelance medical writer based in Cascais, Portugal. She helps pharma, biotech, and meddev companies communicate with their audiences in a clear, accurate, and compelling way. Diana is an active member of the European Medical Writers Association, where she volunteers for the webinar team.

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This week, less is more

First, we go local, with two announcements from the European Medicines Agency (EMA). Then, an article about the micro level checks on which existing molecules can be repurposed to treat SARS-CoV-2. Lastly, a Science article reveals that excipients (drug...

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