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Upcoming sickle cell gene therapies cost effective at $2 million, says ICER

Pharmaceutical Technology

Although the findings in the report are only preliminary, they shed light at the considerations behind the high price tags of gene therapies. As per ICER, if a treatment improves quality of life or extends a patient’s life, then this can be represented in additional QALYs provided by the therapy.

FDA 59
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PharmDs – Crucial to Chronic Care Management Services: A Doctor’s Perspective

PharmD Live

With the challenging number of diagnoses and medications that Medicare patients take, it is essential to have a team member whose primary function is to rapidly review patients records, give informed advice on any side effects to watch out for, and give medication interaction alerts to the rest of the care team.

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Twenty Women Leaders In Healthcare Industry

PharmaShots

Additional Information: Angela started a podcast series Diverse Perspectives where she interviews thought leaders from around the world who are bringing about change in a range of industries. Hatfield Economic Fellow at Cornell University in 2022. Birthplace: She spent her childhood in South Africa. LinkedIn Total experience: 27 yrs.

FDA 40
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Ep. 008 – Vlad Mkrtumyan Podcast Transcript

Pharma Marketing Network

Don ( PMN): Yeah and that might be a concern for some folks out there that who’s websites are supported by advertising because you’re relying upon another third-party that can be adding load time to a site when you’re when you’re add tags are loading.

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Osteopathic Medicine and Surviving Your Second Year of Medical School with Dr. Bryce Brohol ?

The Physician Pharmacist

Nathan and Dr. Brohol offer valuable advice and insights for aspiring medical students, and their personal experiences provide a relatable perspective on the challenges and rewards of pursuing a career in medicine. And they were the one kind of using their expertise to really guide the treatment of the patient.

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Moving to component management & traceability: progress, barriers, and the way forward

pharmaphorum

The process starts adding fields to regulatory submission templates that will incorporate re-used information, then building templates with standardized structures and including structured data tags and sources. Having worked in several organizations of different sizes, he provides perspectives from sponsors, vendors and now CROs.

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Putting complex medicines under the microscope

European Pharmaceutical Review

Crucially, these insights can be applied across the pipeline to help more complex medicines reach the market, for patient benefit. . It is vital to ensure adequate exposure in the target tissue, tailoring product performance to patient needs and the properties of the molecule and target. What constitutes a complex medicine?