Pharma Marketing Network

JULY 10, 2023

Pharmaceutical marketing is the process of communicating the benefits of a pharmaceutical product to potential patients and healthcare providers. Direct-to-physician (DTP) advertising: DTP advertising is advertising that is directed to healthcare providers. This can help patients make informed decisions about their healthcare.

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Healthcare Healthcare Marketing Pharma 40

European Pharmaceutical Review

MAY 7, 2024

major drivers for the injectable drug delivery market include a greater advancement in technology” The research also shared that major drivers for the injectable drug delivery market include a greater advancement in technology, more widespread chronic disease, and higher funding from government around the world.

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Food and Drug Administration Marketing Government Food 69

PM360

AUGUST 9, 2022

Brand Beat: Juul Fights FDA Ban. Shortly after banning Juul from selling its products, the FDA placed a hold on its decision in order to review the company’s case more closely. however, the company is required to prove to the FDA that their e-cigarettes in fact benefit the public. FDA Update. Drug Approvals.

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Healthcare Healthcare Food and Drug Administration FDA 52

pharmaphorum

JANUARY 11, 2023

The filing with the European Medicines Agency (EMA) is based on the results of the phase 2b Study 201 – which supported the approval of lecanemab as Leqembi by the FDA under its accelerated pathway – as well as data from the ongoing phase 3 CLARITY-AD study. The post After FDA nod, Eisai and Biogen file lecanemab in EU appeared first on.

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pharmaphorum

JUNE 27, 2022

Jennifer Mathieu, director of government relations at the Academy of Managed Care Pharmacy (AMCP), tells us why the organisation backed the pre-approval information exchange (PIE) Act of 2022 and how the legislation will empower companies to share information with healthcare payers and plans during the FDA approval process. .

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Food and Drug Administration Medical Patients FDA 75

European Pharmaceutical Review

MARCH 12, 2024

Regulatory bodies such as the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) place great importance on data integrity in the pharmaceutical/life science industry. There is growing awareness of the importance of implementing robust data governance frameworks and compliance programmes to ensure the integrity of data.

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Government Pharma Ethics Training 89

Pharmaceutical Technology

JULY 21, 2022

The pharma industry has deeply rooted environmental, social, and governance (ESG) issues that challenge sustainability. Listed below are the key technology trends impacting the ESG performance in the healthcare sector, as identified by GlobalData. Orthopaedic companies have been using 3D printing for their implants for years.

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Food and Drug Administration Government Pharma Healthcare 98

European Pharmaceutical Review

DECEMBER 21, 2022

The US Food and Drug Administration (FDA) created live biotherapeutic products (LBP) as a new category in the 2012 guidelines. 1 The European Directorate for the Quality of Medicines & Healthcare (EDQM) also accepted LBP as a new category of medicinal products for the European market in 2019.

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Food and Drug Administration FDA Medicine Government 101

pharmaphorum

JUNE 22, 2022

The reason the US government is worried about the supply of pharmaceuticals is immediately clear, a problem securing access to antibiotics, for example, would be a major public health issue. In particular, China is the second largest exporter of drugs and biologics to the US and the largest for medical devices. Security of supply.

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Pharma Manufacturing Government FDA 93

World of DTC Marketing

APRIL 19, 2021

A real conspiracy actually exists, and it is usually uncovered by journalists, whistleblowers, document dumps from a corporation or government, or it’s discovered by a government agency. . They have been tested per the FDA, and to die, those who have been vaccinated have less than a.008% They are a huge threat to healthcare.

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Government Education Side effects Pharma 190

Rep-Lite

APRIL 4, 2024

Sales representatives play a crucial role in connecting healthcare facilities with innovative technologies that improve patient care. This knowledge allows you to speak confidently with healthcare professionals and address their specific needs. Pay close attention to the challenges and priorities of healthcare providers.

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Medical Sales Interpersonal Skills Ethics 52

Pharmaceutical Technology

APRIL 3, 2023

Eisai and the National Cancer Center have signed an agreement to partner on investigator-initiated clinical research for the anti-cancer agent, tazemetostat (Tazverik Tablets 200 mg), based on the Patient-Proposed Healthcare Services system.

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Insurance Government Safety Patients 98

Nixon Gwilt Law

DECEMBER 16, 2021

What can Healthcare and Life Sciences businesses and investors anticipate for the healthcare industry in 2022? We asked our team five direct questions about innovations in healthcare, life sciences, and digital health in the coming year: What healthcare trends or opportunities are you most excited about?

Healthcare 52

Healthcare Healthcare Food and Drug Administration Ethics 52

Pharmaceutical Technology

JANUARY 31, 2023

FDA director Robert Califf gave his prognosis for the pharma industry at this year’s JP Morgan Healthcare Conference in San Francisco over January 9–12. This “skinny” bill passed just in time to continue funding the FDA, with few of the planned amendments. billion in funding, a $226 million increase on the previous year.

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Pharmaceutical Technology

JULY 12, 2022

Novavax has signed an agreement with the US Department of Health and Human Services (HHS), in partnership with the Department of Defense, under which the US government will procure 3.2 Presently, the EUA application for the vaccine submitted by the company is being reviewed by the FDA.

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Food and Drug Administration FDA Government Physicians 64

Pharmaceutical Technology

APRIL 17, 2023

The company announced that Health Canada’s acceptance follows the acceptance by the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA). Pfizer also stated that RSV is the most common respiratory viral pathogen among young children and infants.

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Food and Drug Administration Government Medicine Food 64

Pharmaceutical Technology

OCTOBER 5, 2022

Bringing an end to a 13-year deliberation on a whistleblower lawsuit, Biogen recently agreed to pay a $900 million settlement , amidst increased government alertness on pharmaceutical fraud. The US government has recently prioritized the pursuit of cases such as Biogen’s as a warning to the industry to remain in compliance of the law.

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Government Specialization Physicians Education 59

Pharma Marketing Network

MAY 3, 2023

First, it is important to understand the different regulatory agencies that govern pharmaceutical marketing. The United States Food and Drug Administration (FDA) is the primary regulatory agency that oversees the approval, promotion, and advertising of drugs.

Safety 52

Safety Food and Drug Administration Pharmaceutical Marketing 52

pharmaphorum

AUGUST 19, 2022

It will provide a low-cost online consultation and prescription medicine service to patients, starting with the two oral COVID-19 antivirals – Pfizer’s Paxlovid (nirmatrelvir/ritonavir) and Merck & Co’s Lagevrio (molnupiravir) – which are authorised for at-home use by the FDA.

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Prescription Healthcare Healthcare Healthcare Provider 87

European Pharmaceutical Review

DECEMBER 21, 2022

The Dutch government offers a prime example. This US pathway offers early-phase benefits, including greater FDA collaboration. This US pathway is usually leveraged at later stages in drug development and permits sponsors to use surrogate endpoints to get faster FDA approval. Government of Canada. Government of Canada.

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Food and Drug Administration Medicine Food Government 108

PM360

DECEMBER 20, 2023

With its rapidly evolving healthcare system, limited transparency of public information, and language barriers, China has never proven to be an easy market for overseas pharmaceutical companies to enter. Basic Medical Insurance (BMI), the public insurance that is organized and funded by the government, covers nearly all Chinese citizens.

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pharmaphorum

SEPTEMBER 27, 2022

According to a Department of Justice statement , the payment resolves the suit filed on behalf of the federal government by former Biogen employee Michael Bawduniak, under the whistleblower (qui tam) provisions of the False Claims Act. The suit was filed in 2012 by Bawduniak, acting on behalf of the US government.

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Government Doctors Consulting Training 44

pharmaphorum

SEPTEMBER 1, 2022

“We have created the first telehealth company that makes healthcare services available regardless of a patient’s ability to pay. I have always been passionate about improving the efficiency and equity of healthcare. One of my biggest regrets with Zocdoc is that we didn’t do enough to ensure everyone has access to healthcare.

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Medical Prescription Doctors Physicians 94

European Pharmaceutical Review

DECEMBER 13, 2022

They provided this compound to John Hopkins University who received a grant of nearly $4 million from the National Institutes of Health (NIH) for their smoking cessation study in the US – the first time in 50 years the US government has funded a study evaluating a psychedelic compound for therapeutic use.

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Medicine Food and Drug Administration Ethics Government 100

Clarivate

JANUARY 8, 2024

FDA accelerated approval in August, Clarivate projects the drug will see $850 million in sales by 2029. The year 2024 is shaping up to be the best of times and the worst of times for the pharma industry,” said Henry Levy, President, Life Sciences & Healthcare at Clarivate. Granted U.S.

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Marketing Patients Healthcare Healthcare 59

Pharmaceutical Technology

JULY 14, 2022

This analysis covers late April to May and is based on a list of CMOs impacted by regulatory decisions by the US Food and Drug Administration (FDA), European Medicines Agency (EMA), and reimbursement authorities like the UK’s National Institute of Health and Care Excellence (NICE). Consequential FDA and EMA decisions.

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Manufacturing Food and Drug Administration FDA Pharma 52

PM360

APRIL 7, 2023

a company from the University of Illinois at Chicago will be building upon 19 years of research and the first-in-human pilot clinical trial of immunoglobulin drops, while Grifols , a global leader in plasma-derived therapies, committed to funding the development though FDA approval and commercialization. Selagine, Inc. ,

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Healthcare Healthcare Government Consulting 52

Nixon Gwilt Law

SEPTEMBER 7, 2023

However, as with any emerging area of healthcare innovation, new legal and regulatory considerations arise that must be thoughtfully addressed. While VR holds significant promise, the long-term effects on pediatric populations are not yet fully understood and it can be hard to quantify long-term benefits or risks to the FDA.

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Food and Drug Administration Education Insurance Healthcare 52

European Pharmaceutical Review

MARCH 2, 2023

Time to review data governance Supply chain issues, driven by the pandemic, continue to present problems for the pharmaceutical industry situation that was exacerbated during the winter, with demand at an all-time high. But this requires more proactive data governance, if companies are to truly harvest the power of their data.

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Food and Drug Administration Government Management Medicine 85

Clarify Health

JANUARY 12, 2022

From FDA regulatory approvals to commercialization strategies to value demonstrations, real-world evidence (RWE) plays a pivotal role in the product lifecycle of diagnostics, medical devices, and digital therapeutics (DTx).

Medical 52

Medical Physicians Marketing Education 52

Clarify Health

APRIL 15, 2021

Addressing the challenges of underdiagnoses when launching a rare disease drug Within the past decades, the government has pushed regulatory and financial incentives to encourage the development of rare disease drugs. And 95% of rare diseases do not have any FDA-approved therapeutic. Clinically, NASH is difficult to diagnose.

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FDA Patients Healthcare Provider Government 52

European Pharmaceutical Review

SEPTEMBER 29, 2022

The US Food and Drug Administration (FDA)’s Center for Drug Evaluation and Research (CDER) through the Office of Pharmaceutical Quality in 2021 embarked on an initiative to develop a framework for establishing a pharmaceutical manufacturing site quality rating system, the Quality management maturity (QMM) programme.

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Management Food and Drug Administration Manufacturing Pharmaceutical manufacturing 77

Clarify Health

OCTOBER 26, 2021

Food and Drug Administration (FDA) released guidance entitled, Enhancing the Diversity of Clinical Trial Populations — Eligibility Criteria, Enrollment Practices, and Trial Designs Guidance for Industry. To advance equity in clinical research, the U.S. In fact, 73% were White, 14% were Asian, 6% were Hispanic, and 5% were African American.

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Food and Drug Administration Recruitment Pharmaceutical manufacturing Medical 52

Legacy MEDSearch

NOVEMBER 6, 2023

Histotripsy has been shown to be safe and effective in destroying targeted liver tumors, including unresectable liver tumors, recently gaining clearance from the FDA to market the Edison System for the non-invasive destruction of liver tumors, using a non-thermal, mechanical process of focused ultrasound.

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Recruitment Physicians Medical Patients 52

European Pharmaceutical Review

AUGUST 23, 2022

The US Food and Drug Administration (FDA) further estimates that 97 percent of online pharmacies are operating illegally. We believe that we need more scientists and researchers to work effectively at the intersection of academia, pharmaceutical companies and government agencies. About the author.

Medicine 91

Medicine Food and Drug Administration Pharmaceutical products Pharmaceutical 91

Clarivate

OCTOBER 30, 2022

Amid an escalation in the marketing of digital therapeutics (DTx) that diagnose, treat and/or manage health conditions in the United States, the federal government has yet to establish a coverage policy for these software-based interventions for the Medicare population. As a result, few products have FDA clearance. What’s next?

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Insurance FDA Prescription Marketing 52

European Pharmaceutical Review

APRIL 13, 2023

The Schedule 1 classification means that these substances cannot be administered by doctors and, though they may be used for the purposes of research a government licence is often required. The US Food and Drug Administration (FDA) has decided to fast-track psilocybin for depression, with full support from President Biden’s administration.

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Medicine Food and Drug Administration Doctors Government 115