pharmaphorum

NOVEMBER 16, 2021

. “The FAD is a significant milestone for cenobamate and takes us closer towards reimbursement in England and Wales,” commented Stuart Mulheron, general manager UK & Ireland, Angelini Pharma. An opinion from the Scottish Medicine Consortium (SMC) on the use of the drug by NHS Scotland is expected to be published early in 2022.

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Documentation 94

Pharmaceutical Technology

MAY 2, 2023

Combining data from all markets, efficacy-related needs were identified as the most important unmet needs category. IO therapies come with a hefty price tag, with ICI therapies in the US typically exceeding $100,000, while cell therapies can exceed $400,000. Cost-related unmet needs also scored highly.

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Immunization Vaccines 52

pharmaphorum

JUNE 8, 2021

That was the damning conclusion of the influential Institute for Clinical and Economic Review (ICER) in the US to yesterday’s approval of Aduhelm (aducanumab), the first new treatment for Alzheimer’s since 2003, which it says has “no evidentiary basis.” — Dr. Patrizia Cavazzoni (@FDACDERDirector) June 7, 2021.

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FDA Labelling 98

Pharmaceutical Technology

JUNE 29, 2022

The US Food and Drug Administration (FDA) put a high-profile bluebird bio trial for sickle cell disease on partial clinical hold, and advisory panels deliberated over decisions involving gene therapies for amyotrophic lateral sclerosis (ALS), cerebral adrenoleukodystrophy (CALD), and beta-thalassemia.

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Pharmaceutical Companies Pharmaceutical Companies FDA 98

PharmD Live

DECEMBER 21, 2021

Aduhelm was approved by the FDA in 2021 with clinical trials outcome data indicating the potential to slow the accumulation of amyloid plaques. With an annual price per patient of nearly $56,000 per year, patients’ families are looking for solutions for their loved ones–with a huge price tag. Aduhelm earns FDA approval.

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FDA Hospitals 52

The Checkup by Singlecare

NOVEMBER 2, 2023

The alarming increase in obesity rates heightens the need for effective weight management solutions. If a drug is FDA approved for a particular purpose, that means the Food and Drug Administration (FDA) has deemed the drug to be effective for that purpose, based on reviewing extensive data from clinical trials supporting its use.

Insurance 52

Insurance FDA Adverse Reactions Hospitals 52

The Checkup by Singlecare

MARCH 21, 2023

Compare hydrocodone acetaminophen alternatives | Belbuca | Methadose | Cymbalta | Naprosyn | Qdolo | Natural alternatives | How to switch meds The management of pain is a sensitive and sometimes controversial topic. It is a personal experience, and access to pain management is a basic right.

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Dosage Controlled Substances Labelling Packaging 52

Pharmaceutical Technology

MARCH 22, 2023

The pharmaceutical industry began using radio frequency identification (RFID) tags in the early 2000s. Pfizer was the first to use the tech, adding RFID tags to track a Viagra (sildenafil) shipment circa 2006. Twenty years ago, the cost of implementing RFID tags and the ecosystem (software) was much more expensive than today.

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Labelling Data Entry Communication FDA 105

pharmaphorum

SEPTEMBER 30, 2022

Component management is fairly new to the regulatory market, with pharmaceutical firms moving from traditional document management systems to more dynamic component content management systems. Most of the information is submitted in the form of unstructured PDF documents, with data embedded into them.

Documentation 52

Documentation Pharmaceutical Companies Pharmaceutical Companies 52

PharmaShots

MARCH 9, 2023

An elected member of Association of American Physicians (AAP) and the American Society for Clinical Investigation (ASCI), she also serves fellow of the American Gastroenterological Association. Education: She graduated from Cornell University with a master’s in Business Administration and Management.

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FDA Pharmaceutical Companies Pharmaceutical Companies Immunization 40

Pharmaceutical Technology

JUNE 21, 2023

The high price tag may be hard to defend , but with lifetime treatment costs for haemophilia B reaching as high as $23m for some, the single-dose treatment could prove far more cost-effective. Despite this, the Institute for Clinical and Economic Review (ICER) claimed that a fairer price would be in the region of $2.9m.

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FDA 98

pharmaphorum

JUNE 15, 2021

The adoption of New Science – a unique combination of the best in science and health technology that address significant unmet patient needs – is delivering more precise and effective treatments, but often at a higher price tag, according to new research. And governments struggle to manage costs.

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Vaccines 90

pharmaphorum

OCTOBER 4, 2022

Central to the initiative is the aim to gather data from willing participants that can provide greater insights into cancer development and treatment over time. The Moonshot was started with three aims: to accelerate scientific discovery in cancer, foster greater collaboration between stakeholders, and to improve the sharing of cancer data.

Documentation 102

Documentation Data Entry HIPAA Insurance 102

The Checkup by Singlecare

MAY 8, 2023

Compare tramadol alternatives | Belbuca | Cymbalta | Naproxen | Celebrex | Voltaren gel | Natural alternatives | How to switch meds We have all experienced pain at some point and can therefore understand that the scale of pain ranges from a manageable ache to uncomfortable to, frankly, excruciating.

Controlled Substances 52

Controlled Substances Dosage Labelling FDA 52

Viseven

FEBRUARY 6, 2023

In addition, AI-driven software attracts pharma companies that study its potential in new drug discovery, patient diagnostics automation, and clinical trials which is great for recruitment campaigns. What should healthcare marketers do? The world does not stand still, and no one should, especially pharma marketers.

Communication 75

Communication 75

The Physician Pharmacist

SEPTEMBER 14, 2023

He notes that there is no clinical difference between the two, but that osteopathic physicians are required to complete several hundred hours of osteopathic manipulative medicine practice in school. I in that I did a Clinical Oncology rotation at the Johns Hopkins Hospital in Baltimore, and hated it. So where they were getting a 4.0,

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Medical Schools Hospitals Communication Patient Care 52

European Pharmaceutical Review

DECEMBER 27, 2023

2,3 Clinical implementation of CAR T-cell technology requires a reproducible T-cell manufacturing platform, which necessitates effective gene-transfer tools and T-cell culture conditions. 6-8 Clinical recommendations also change. This is in addition to its considerable price tag.

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Adverse Reactions Immunization Medical Schools Chemotherapy 83

Pharmaceutical Technology

NOVEMBER 30, 2022

Several other treatments, like Novo Nordisk’s CagriSema (semaglutide + cagrilintide), are expected to follow after showing encouraging Phase II data. In the past, obesity medications were often dismissed due to insufficient efficacy data and the fact that they were associated with a high occurrence of side effects. More data needed.

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Insurance Labelling Communication FDA 105

Pharmaceutical Technology

NOVEMBER 30, 2022

Several other treatments, like Novo Nordisk’s CagriSema (semaglutide + cagrilintide), are expected to follow after showing encouraging Phase II data. In the past, obesity medications were often dismissed due to insufficient efficacy data and the fact that they were associated with a high occurrence of side effects. More data needed.

Insurance 98

Insurance Labelling Communication FDA 98

Pharma Marketing Network

JUNE 8, 2020

There’s what I call the real market and so this market really exploded, and I have data in this chapter about it. But I guess to be a bit of a contrarian and backed up with a lot of data. You better get people to a Virginia Mason or a Mayo Clinic or things like that. I mean Mayo Clinic, they found about 20% misdiagnosis.

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Health and Personal Care Stores Hospitals Mayo Clinic Specialty Pharmacies 40