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Roche Receives the US FDA’s Approval for HPV Self-Collection Solutions for Cervical Cancer

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Roche Receives the US FDA’s Approval for HPV Self-Collection Solutions for Cervical Cancer

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  • Roche has received the US FDA’s approval for its human papillomavirus (HPV) self-collection solution with its cobas HPV test to detect cervical cancer at the earliest for the treatment
  • The HPV self-collection solution works by screening vaginal samples from the individuals which are sent to labs for analysis through Roche’s cobas molecular instrument to detect if the patient is HPV positive or not for further treatment
  • Additionally, Roche teamed up with the National Cancer Institute (NCI) for the Cervical Cancer “Last Mile” Initiative, facilitating the regulatory approval process

Ref: Roche | Image: Roche

Related News:- Roche to Highlight the P-III (OCARINA II) Trial Results of Ocrevus for Treating Progressive and Relapsing Multiple Sclerosis at AAN 2024

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Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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