Regulatory affairs (RA) provides a crucial link between pharma companies and regulatory authorities. Without the RA department, pharma companies couldn’t bring any drugs to market because they’d be unable to meet the required legislation to licence their products.

RA departments need scientists to collate and evaluate scientific data, write clear arguments and explanations for new product licences/licence renewals/licence variations, and prepare submissions. These scientists work as medical writers, preparing all the documentation needed for RA.

But what exactly does an RA Medical Writer do? And how can you break into RA?

In this video, Vera Chan (host of PhD Coffee Time: [ Ссылка ], and medical writer in RA), answers these questions and more about working in RA.

Useful Resources

Download a free checklist of what to include in medical writing tests in order to pass, and receive regular updates about life as a medical writer and tips for transitioning from academia to pharma through the BB newsletter:

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Music Credits Song: Jarico - Island (Vlog No Copyright Music) Music promoted by Vlog No Copyright Music. Video Link: [ Ссылка ]

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