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Dr Reddy's Launches Migraine Management Device 'Nerivio' In Europe

Nerivio is approved by the USFDA, and is CE-mark certified in Europe.

<div class="paragraphs"><p>Nerivio is approved by the US Food and Drug Administration. (Source: Company website)</p></div>
Nerivio is approved by the US Food and Drug Administration. (Source: Company website)
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Dr Reddy’s Laboratories Ltd. on Wednesday said it has launched migraine management wearable device Nerivio in Germany through its step-down subsidiary Betapharm. The launch marks the company’s entry into digital therapeutics in Europe, the Hyderabad-based drug major said in a statement.

Nerivio is approved by the US Food and Drug Administration (USFDA), and is CE-mark certified in Europe. Dr Reddy’s launched Nerivio in India last year.

Nerivio has had an encouraging start in India, with recommendations from neurologists in India and bringing relief to patients living with migraine, Dr Reddy’s CEO of Branded Markets (India and Emerging Markets) MV Ramana said.

'We believe this product meets a genuine unmet clinical need among migraine patients, and has the potential to reduce pill burden in migraine,' he added.

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