Salesforce

SEPTEMBER 16, 2022

Two patients with the same diagnosis, prescribed the same medical regime, and treated by the same doctor in the same hospital could have wildly different outcomes. Examining your patients’ health within the context of their lives is critical. What do trusted healthcare organizations do differently? Read the report.

Patients 52

Patients Healthcare Healthcare Food 52

Pharmaceutical Technology

OCTOBER 7, 2022

The US Food and Drug Administration (FDA) is presently reviewing teplizumab for the delay of clinical T1D in people who are at risk. If approved, Sanofi US will leverage its existing world-class capabilities in diabetes care to enhance efforts in both patient and healthcare provider access.”.

Food and Drug Administration 119

Food and Drug Administration FDA Healthcare Provider Prospecting 119

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.

Healthcare 40

Healthcare Healthcare Marketing Pharma 40

World of DTC Marketing

SEPTEMBER 17, 2020

IN SUMMARY: American healthcare is failing. While there are lots of reasons for this the silence of healthcare providers is a huge reason. If that doesn’t work then patients who are obese need to pay more for health insurance, plain and simple. We need to do to obesity what we did for smoking.

Healthcare 242

Healthcare Healthcare Insurance Healthcare Provider 242

Pharmaceutical Technology

APRIL 28, 2023

Otsuka America Pharmaceutical and Lundbeck have received approval from the US Food and Drug Administration (FDA) for a new drug application for Abilify Asimtufii (aripiprazole) to treat schizophrenia or for maintenance monotherapy treatment of bipolar I disorder in adult patients.

Food and Drug Administration 52

Food and Drug Administration FDA Healthcare Provider Food 52

Pharmaceutical Technology

AUGUST 12, 2022

In June this year, it was announced that the US Food and Drug Administration (FDA) had granted UK-based OxfordVR a breakthrough device designation for its gameChangeVR treatment to deliver immersive cognitive behaviour therapy (CBT) to people suffering from schizophrenia and other mental illnesses. million people in the UK and 2.7

Food and Drug Administration 141

Food and Drug Administration Pharmacology Side effects Physicians 141

Clarivate

MARCH 14, 2024

Over the past few years nitrosamines and nitrosamine impurities have been increasingly gaining the reputation of being high-risk containments in the food industry. The food sector has already initiated the publication of preliminary regulations aimed at restricting PFAS in packaging. [3].

Pharmaceutical 52

Pharmaceutical Manufacturing Food Healthcare Provider 52

Pharmaceutical Technology

JUNE 2, 2023

Kicking off this year’s American Society of Clinical Oncology’s (ASCO) conference, Novartis has released data supporting the use of its CDK4/6 inhibitor Kisqali (ribociclib) as an adjuvant treatment for a group of early-stage breast cancer patients.

Food and Drug Administration 52

Food and Drug Administration Healthcare Provider Patients Food 52

Pharmaceutical Technology

DECEMBER 5, 2022

Incyte could also grant a potential licence to CMS for other topical formulations of ruxolitinib to treat ailments, such as vitiligo and atopic dermatitis, in the future, for patients in mainland China, Hong Kong, Macau, Taiwan and some Southeast Asia nations.

Food and Drug Administration 52

Food and Drug Administration Healthcare Provider Food Patients 52

Legacy MEDSearch

AUGUST 16, 2023

Food and Drug Administration (FDA) for the indication of diagnosing Electrographic Status Epilepticus (ESE). per eligible Medicare patient case. ClarityPro is now the only FDA-indicated device for the diagnosis of ESE in adult patients over the age of 18. Ceribell, Inc. NTAP reimbursement of up to $913.90

FDA 52

FDA Food and Drug Administration Healthcare Provider Recruitment 52

Impetus Digital

AUGUST 12, 2022

They will also dive into topics related to patient-centricity and digital technologies in Pharma, including how these can be used to support HCPs and patients during this challenging time. Impetus Digital is the spark behind sustained healthcare stakeholder communication, collaboration, education, and insight synthesis.

Medical 52

Medical Professional Services Medical science Healthcare Provider 52

PM360

APRIL 18, 2023

ISPOR Summits draw healthcare stakeholders with an interest in HEOR-related topics, including researchers and academicians, assessors and regulators, payers and policymakers, the life sciences industry, healthcare providers, and patient engagement organizations. Speakers include: Moderator: Marc Berger, MD; Marc L.

Food and Drug Administration 96

Food and Drug Administration Healthcare Healthcare Food 96

LEVO Health

MAY 10, 2023

With strict regulations and a rapidly evolving landscape, healthcare marketing requires a diverse and skilled team. However, with the right approach, you can create a strong marketing strategy that not only complies with regulations but also enhances patient engagement and drives growth for your practice.

Healthcare 52

Healthcare Healthcare Marketing Healthcare Provider 52

Impetus Digital

FEBRUARY 16, 2024

Based on our survey of hundreds of healthcare provider advisors in 2022–2023, over three-quarters stated that they prefer virtual/hybrid meetings, with the convenience and flexibility of digital meetings rated as the top benefits (unpublished data). I’ve said it before, and I’ll say it again: virtual is here to stay.

Pharma 84

Pharma Healthcare Provider Healthcare Healthcare 84

Legacy MEDSearch

DECEMBER 1, 2022

HemoSonics, LLC , a leading medical device company delivering individualized diagnostic solutions for Patient Blood Management (PBM), announced that it has received 510(k) market clearance from the U.S. Food and Drug Administration (FDA) for the Quantra Hemostasis System with QStat Cartridge. market today.

FDA 95

FDA Food and Drug Administration Recruitment Medical 95

PM360

MARCH 22, 2024

Think about patients who need treatment multiple times per day versus you get an infusion and then you’re good to go for multiple years.” Polycystic Kidney Disease is a genetic condition that results in cysts on the kidneys which grow and often result in kidney failure by the time the patient is in their late 40s or 50s.

Food and Drug Administration 52

Food and Drug Administration FDA Healthcare Healthcare 52

Legacy MEDSearch

NOVEMBER 28, 2022

Food and Drug Administration for commercial use in the United States. The BodyTom 64 brings the power of innovative imaging to patients’ bedsides safely and efficiently. the healthcare subsidiary of Samsung Electronics Co., NeuroLogica Corp.,

FDA 92

FDA Food and Drug Administration Electronics Recruitment 92

Clarify Health

OCTOBER 10, 2023

When building provider networks, it is crucial to include providers who can assess and address social determinants to ensure that care is equitable, patient-centered, and effective in improving health outcomes and reducing healthcare disparities.

Networking 59

Networking Education Healthcare Healthcare 59

Pharmaceutical Technology

JULY 20, 2022

On 6 July, in an effort to accelerate access, the US Food and Drug Administration (FDA) allowed pharmacists to also begin prescribing the drug to eligible individuals with Covid-19. And, if there are concerns, the pharmacist can call their healthcare provider to develop a plan.

Food and Drug Administration 111

Food and Drug Administration Physicians Prescription Medical 111

European Pharmaceutical Review

SEPTEMBER 2, 2022

This can be achieved by reducing the burden of adverse reactions or by optimising benefits through patient selection (eg, contraindications, recommendations of use, warnings, concomitant medicine[s], or certain test parameters) and treatment management (eg, specific dosing regimen, relevant testing, patient follow-up).

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Food and Drug Administration Medicine Safety Food 75

PM360

JUNE 29, 2022

Healthcare and pharma companies are watching this trend and refining their strategies to meet tomorrow’s health consumer. But to succeed, players must deeply understand both the end-to-end consumer and patient experience and create an ecosystem of partners to deliver the care, products, and experiences that health-conscious consumers need.

Retail 97

Retail Healthcare Healthcare Marketing 97

Impetus Digital

JULY 15, 2022

However, with flight , gasoline , and food prices skyrocketing lately, in-person engagements are becoming more expensive and may not be the best “bang for your buck.” If anything, it is more crucial than ever to gather insights from healthcare providers, payers, and patients on current market conditions.

Healthcare Provider 95

Healthcare Provider Food Pharma Healthcare 95

PM360

OCTOBER 24, 2022

GoodRx’s mission is to provide Americans—regardless of income or insurance status—the knowledge, choice, and care they need to stay healthy by improving access to affordable healthcare. Trusted by over 100 million patients and 825,000 providers, GoodRx ranks #1 in consumer trust of digital healthcare brands.

Insurance 40

Insurance Prescription Healthcare Healthcare 40

pharmaphorum

OCTOBER 19, 2022

People enjoy when products and services come to them (and fast) — healthcare included. Instead of patients travelling to doctors, doctors will now visit patients so that people receive the care they need in the place they’re most comfortable: their own homes. What are the opportunities for CVS and the healthcare industry? .

Healthcare 52

Healthcare Healthcare Retail Insurance 52

Legacy MEDSearch

JULY 13, 2022

Food and Drug Administration (FDA) has granted Breakthrough Device Designation to the AccuCinch ® Ventricular Restoration System. This program is designed to ensure patients and healthcare providers have more timely access to these medical devices. Ancora Heart , Inc., An estimated 6.5 million U.S. An estimated 6.5

Food and Drug Administration 52

Food and Drug Administration FDA Medical Recruitment 52

Pharmaceutical Technology

MARCH 22, 2023

Healthcare providers are under pressure to address the growing issue of substance use disorders. The device received Breakthrough Device Designation from the US Food and Drug Administration (FDA) in December 2020 as no standard of care for the condition existed.

Food and Drug Administration 52

Food and Drug Administration Healthcare Healthcare Medical 52

Healthcare Success

DECEMBER 6, 2022

Combine that with a steady decline in private practice physicians due to patient volume loss, revenue loss, and increased medical supply costs—and disruptors are deftly filling in the cracks they’ve left behind. Patients Consumers are researching online, and their searches are becoming more sophisticated. Google Business Profile.

Healthcare 112

Healthcare Healthcare Marketing Competition 112

Clarivate

APRIL 24, 2023

Health systems will buy or establish an insurance plan to serve as an extension of their continuum of care, a means of directing referral streams to increase revenue and securing control over clinical and formulary decisions for patients.

Healthcare 89

Healthcare Healthcare Marketing Physicians 89

pharmaphorum

JANUARY 24, 2023

Ben Hargreaves finds that the vast amount of genetic data that exists today could help provide a faster, more targeted way of developing new drug candidates. Recent years have brought a revolution to the way in which patients receive treatment. Though instances of this kind of therapy are rare, it is a growing area.

Food and Drug Administration 86

Food and Drug Administration Pharma Medicine Healthcare 86

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.

Food and Drug Administration 52

Food and Drug Administration Recruitment Pharmaceutical manufacturing Medical 52

Nixon Gwilt Law

APRIL 22, 2024

Valid: Confirms that DSIs are scientifically and statistically sound, providing reliable predictions based on the data and methodologies employed. Effective: Ensures that DSIs achieve their intended outcomes, improving clinical decision-making and patient care.

Healthcare 52

Healthcare Healthcare Training Food and Drug Administration 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. Acknowled gement.

Management 77

Management Food and Drug Administration Manufacturing Pharmaceutical manufacturing 77

PM360

JUNE 16, 2023

The Role of the COVID-19 Pandemic on the Diagnostics Market Landscape Diagnostic testing has always been seen as a valuable tool for healthcare providers (HCPs) to accurately diagnose illness and ensure that patients receive necessary medical care.

Marketing 52

Marketing Healthcare Healthcare Medical 52

Impetus Digital

OCTOBER 20, 2022

Based on over a decade of feedback from thousands of healthcare provider (HCP) advisors, across all therapeutic areas, we are consistently hearing that asynchronous virtual touchpoints (AVTs) on the Impetus InSite Platform® are the #1 preferred way of engaging with Big Pharma. About Impetus Digital.

Healthcare Provider 84

Healthcare Provider Transportation Pharma Healthcare 84

pharmaphorum

JANUARY 24, 2023

For the most commonly used, high volume medicines, countrywide networks of distribution to get them to where patients live, reliably, securely, and regularly, are required. Healthcare has a substantial carbon footprint, approximately 4% of global emissions and, of that, medicines generate up to one third.

Medicine 92

Medicine Healthcare Healthcare Pharma 92

European Pharmaceutical Review

NOVEMBER 8, 2022

In the US, members of the public can request, through a Citizen Petition, that the US Food and Drug Administration (FDA) “take or refrain from taking” various administrative actions, including denying approval of generic and biosimilar drug applications. Citizen Petitions before the FDA. Measuring and rating biosimilar access. Conclusion.

Food and Drug Administration 52

Food and Drug Administration Pharma Prescription Manufacturing 52

Vodori

MAY 27, 2022

The pandemic has shaken the pharma sales channel and required companies to rethink their digital patient and HCP marketing strategies. Healthcare providers and sales reps alike had to get word out under unprecedented constraints, and digital fit the bill.

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Management Healthcare Provider Sales Healthcare 52