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6 Digital Health Takeaways From CES 2022 That Will Change Healthcare as We Know It

Intouch Solutions

Ford discussed his vision and the promise of healthcare technology: to bring care that’s more personal and precise, proactively manage health, detect disease early, and even prevent it from happening in the first place. Why This Matters for Pharma It’s critical to evaluate patient and HCP experiences in the context of a virtual care setting.

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Supporting and empowering carers to make their voices heard

pharmaphorum

In facts, caregivers often take on the task of searching for the best pathways for those they care for; also, they have to learn to provide care to their assisted ones, which is no simple undertaking. In a patient intelligence research project conducted by PIPHealth in 2020, the importance of the carer’s voice came to light.

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The US biosimilar market: Predictions for 2021

pharmaphorum

It has been five years since the first biosimilar launched in United States market—marking the first steps in expanding access to innovative biologic-based treatments that help patients manage and treat difficult illnesses such as cancer, rheumatoid arthritis, and other life-altering diseases. million patients. million patients.

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Patient centricity and the changing pharmaceutical vista

pharmaphorum

Having previously spoken with Dr Mullen three years ago when she was country medical director for the UK & Ireland at GSK – on the topic of patient centricity and embedding that focus within the core of a pharmaceutical company – our recent interview provided some interesting insights into the changing landscape of the industry.

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Pfizer Receives Positive CHMP Opinion for Conversion of PAXLOVID™ Conditional Marketing Authorization to Full Marketing Authorization in the European Union

Pfizer

This opinion from the CHMP confirms that the benefits of PAXLOVID in helping to reduce severe COVID-19-related outcomes, including hospitalization and death, in high risk patients continue to outweigh its potential risks. The European Commission (EC) will review the CHMP recommendation and is soon expected to make a final decision.

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Pfizer to Provide U.S. Government with an Additional 3.7 Million Treatment Courses of PAXLOVID™ to Help Combat COVID-19

Pfizer

PAXLOVID plays an important role in helping to combat COVID-19-related hospitalizations and death in high-risk patients. Food and Drug Administration (FDA) for approval of PAXLOVID for patients who are at high risk of progression to severe disease from COVID-19. (NYSE: PFE) has reached an agreement with the U.S. Government.

Drugs 110
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U.S. FDA Extends Review of Pfizer’s New Drug Application for PAXLOVID™

Pfizer

patients under Emergency Use Authorization as a critical tool in the fight against COVID-19. PAXLOVID is authorized for emergency use by the FDA for the treatment of mild-to-moderate COVID-19 in adults and pediatric patients (12 years of age and older weighing at least 40 kg) who are at high-risk for progression to severe COVID-19.

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