Clear medical WRITING
for pharma, biotech, and medical device companies

Work with me

I’m a pharmacist and medical writer based in Cascais, Portugal who helps life sciences companies create accurate and compliant content.

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Pharma & Biotech have to quickly and effectively produce documents that engage patients and please stakeholders. Medical device companies have to navigate EU MDR and 510k submissions.

I’m an experienced and reliable writer who can work independently or integrate seamlessly with your existing team.

“(…) declared professional medical writing support was associated with more complete reporting of clinical trial results and higher quality of written English. Medical writing support may play an important role in raising the quality of clinical trial reporting.“

Gattrell WT, Hopewell S, Young K, et al

Professional medical writing support and the quality of randomised controlled trial reporting: a cross-sectional study, BMJ Open 2016;6:e010329. doi: 10.1136/bmjopen-2015-010329

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How I work

Every project is different, but there’s an underlying process behind the scenes for each one. To make sure you get consistent projects that are perfectly adapted to you, these are the main steps I follow:

Understand your needs

I take the time to understand your goals: a quick chat or email for the simplest of projects, ongoing updates for longer projects.

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Write the content

This is where I sit down to research, write, and apply all my knowledge to your project.

Deliver and feedback

I deliver my work in time and ask for your honest feedback.

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Say Hello!

Are you struggling with tight deadlines, regulatory constraints or just need great content for your projects?

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