Food and Drug Administration, Physicians and Specialization

FDA grants approval for Amylyx’s Relyvrio to treat ALS

Pharmaceutical Technology

OCTOBER 1, 2022

The US Food and Drug Administration (FDA) has granted approval for Amylyx Pharmaceuticals’ Relyvrio (sodium phenylbutyrate and taurursodiol) to treat adult patients with amyotrophic lateral sclerosis (ALS).

Food and Drug Administration

Food and Drug Administration FDA Prescription Specialization

Pandemic Innovators: Pharma Marketing Strategies that Reinvent the In-Person Conversation

Pharmaceutical Representative Training

DECEMBER 28, 2021

Before 2020, the landscape of drug marketing involved following drug approvals by the Food and Drug Administration ( FDA ), finding which patient population would benefit from therapy, and visiting specialized doctors in-person to advertise its advantages compared to current guidelines.

Marketing

Marketing Food and Drug Administration Pharma Doctors

Lazurite is Recognized in the 2022 Medical Device Network Excellence Awards & Rankings for its ArthroFree™ System

Legacy MEDSearch

DECEMBER 7, 2022

Food and Drug Administration market clearance for the ArthroFree System. This was followed by additional partnerships with Hospital for Special Surgery (HSS) in New York, University Hospitals of Cleveland, and LG Electronics USA.”. “We The company hit an important milestone in March 2022 when it received U.S.

Networking

Networking Medical Food and Drug Administration Recruitment

FDA Approves Innovative 4D Flow MRI Blood Flow Analysis Software from Cardio Flow Design Inc.

Legacy MEDSearch

JUNE 19, 2023

The US Food and Drug Administration has approved the use of iTFlow® in blood flow analysis. Combining advanced algorithms and image analysis techniques assists physicians and healthcare professionals in diagnosis and treatment planning. iTFlow® is an innovative software solution developed by Cardio Flow Design Inc.

FDA

FDA Food and Drug Administration Recruitment Physicians

Clinical Research News: Social Determinants Of Health Data Help Identify Sites For Trials

Clarify Health

NOVEMBER 21, 2022

It has been more than a decade now since the notion of social determinants started expanding to consider access to transportation, food, income, and decent housing on care journeys and outcomes, says Drouin. Clarify Health decided to investigate the tactics deployed by banks and online retailers like Amazon. But the U.S.

Food and Drug Administration

Food and Drug Administration Transportation Food Recruitment

Medical Device Marketing: Targeting the Right Patients at the Right Time

LEVO Health

OCTOBER 26, 2022

Food & Drug Administration (FDA) classifies medical devices. Class II: requires general controls and special controls with and without exemptions and poses a moderate risk. You need to be a trusted partner for both patients and their providers alike. . Bringing Your Medical Device to the Market.

Medical

Medical Marketing Patients Food and Drug Administration

For rare disease patients in Mainland China, hope of greater access to treatment

Clarivate

MAY 24, 2022

Recent policy and regulatory moves have begun to sketch out a framework for rare disease drug approvals in the country, but obstacles to approvals and patient access remain. The list, designed to serve as a reference point for prioritized drug review and evaluation policies, included 121 rare diseases. [8]. 10] [11] [12].

Patients

Patients Food and Drug Administration Marketing Pharma

Clinical Research News: Social Determinants Of Health Data Help Identify Sites For Trials

Clarify Health

NOVEMBER 21, 2022

It has been more than a decade now since the notion of social determinants started expanding to consider access to transportation, food, income, and decent housing on care journeys and outcomes, says Drouin. Clarify Health decided to investigate the tactics deployed by banks and online retailers like Amazon. But the U.S.

Food and Drug Administration

Food and Drug Administration Transportation Food Recruitment

SpectraWAVE Secures 510(k) Clearance of HyperVue™ Intravascular Imaging System

Legacy MEDSearch

MARCH 1, 2023

a medical imaging company focused on improving the treatment and outcomes for patients with coronary artery disease (CAD), today announced Food and Drug Administration (FDA) 510(k) clearance of their flagship intravascular imaging system, HyperVue. SpectraWAVE, Inc., Chief Executive Officer of SpectraWAVE.

Food and Drug Administration

Food and Drug Administration Physicians Recruitment Medical

Private Patient Advocacy: The Medical Sales Rep’s Role In The Nursing World With Antra Boyd And Karen DiMarco, Part 2

Evolve Your Success

MAY 17, 2022

You know when they are trying to push a drug and white-knuckling it. When a physician decides to use a robotic machine, that is not part of my decision-making process and the OR manager. You ask the hospital administrators to figure out the financial aspects of that side of it. What drugs are we using? Sales can be pushy.

Medical sales

Medical sales Medical Sales Patients

Gene therapies transform rare disease treatment: hope for patients amidst regulatory, payer and developer challenges

Clarivate

MAY 24, 2023

Food and Drug Administration advisory committee’s narrow 8-6 vote in favor of recommending accelerated approval for a first-in-class gene transfer therapy was welcomed by Duchenne muscular dystrophy (DMD) patients and caregivers.

Patients

Patients Food and Drug Administration Biopharma FDA

Cardiovascular Medical Device Sales With Marc Toth

Evolve Your Success

FEBRUARY 7, 2023

The CE experience for this Podcast is powered by CMEfy – click here to reflect and earn credits: [link] — Watch the episode here Listen to the podcast here Cardiovascular Medical Device Sales With Marc Toth In this episode, we have with us another special guest and he goes by the name of Marc Toth. Who is Marc Toth?

Medical

Medical Sales Medical sales Doctors

Ep. 001 – John Mack Podcast Transcript

Pharma Marketing Network

JUNE 11, 2020

I was at Physicians Online at the time. You know, in November 2009, the FDA held a public hearing about the promotion of Food and Drug Administrative Related Regulated Medical Products, using the internet and social media tools. They would write up the presentations by physicians about drugs.

Media

Media Pharma Ethics Consulting

Uri Goren

Cadensee

JULY 20, 2021

48:12 What is Uri Gorenseeing that is special in the Israeli Digital Health ecosystem? Basically, I started teaching myself how to get good information outside the internet and see how that empowers us with our discussion with a physician with everything that we did. So, I myself, was kind of tasked with go and search on the internet.

Food and Drug Administration

Food and Drug Administration Doctors Healthcare Healthcare

Pharma Rep Focus

FDA grants approval for Amylyx’s Relyvrio to treat ALS

Pandemic Innovators: Pharma Marketing Strategies that Reinvent the In-Person Conversation

Trending Sources

Lazurite is Recognized in the 2022 Medical Device Network Excellence Awards & Rankings for its ArthroFree™ System

FDA Approves Innovative 4D Flow MRI Blood Flow Analysis Software from Cardio Flow Design Inc.

Clinical Research News: Social Determinants Of Health Data Help Identify Sites For Trials

Medical Device Marketing: Targeting the Right Patients at the Right Time

For rare disease patients in Mainland China, hope of greater access to treatment

Clinical Research News: Social Determinants Of Health Data Help Identify Sites For Trials

SpectraWAVE Secures 510(k) Clearance of HyperVue™ Intravascular Imaging System

Private Patient Advocacy: The Medical Sales Rep’s Role In The Nursing World With Antra Boyd And Karen DiMarco, Part 2

Gene therapies transform rare disease treatment: hope for patients amidst regulatory, payer and developer challenges

Cardiovascular Medical Device Sales With Marc Toth

Ep. 001 – John Mack Podcast Transcript

Uri Goren

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