Pharmaceutical Technology

JULY 28, 2022

Roche’s Susvimo (ranibizumab sustained release formulation) follows a similar theme; patients who are implanted with Susvimo are expected to visit their doctor only twice a year to have the implant refilled so that the medicine can be delivered to their eyes continuously. The therapy received FDA approval in October last year.

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Pharmacy Checkers

JANUARY 10, 2020

This post is mostly a story about a very well manufactured, safe and effective, foreign version of an FDA-approved drug. These drugs are normally far less expensive than the FDA-approved version sold in the U.S. He went to our site to discover that brand-name Livalo ( pitavastatin ). and arguably just as safe.

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The Pharma Data

MAY 19, 2023

ABBOTT RECEIVES FDA APPROVAL FOR TACTIFLEX™ ABLATION CATHETER FOR TREATMENT OF ABNORMAL HEART RHYTHM Abbott (NYSE: ABT) today announced that the U.S. 6 “Abbott is leading the way in helping doctors manage common arrhythmias with the most holistic portfolio for this condition in the world,” said Christopher Piorkowski, M.D.,

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XTalks

FEBRUARY 16, 2023

However, the company last aired the ad on May 2, 2022, the same day they announced the US Food and Drug Administration (FDA) approval of Quviviq. Quviviq is an FDA-approved prescription medicine that helps treat insomnia in adults, with a low risk of dependence and side effects. billion during the same period.

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Pharma Marketing Network

FEBRUARY 19, 2025

Introduction Email marketing remains one of the most powerful tools for pharma brands , helping reach healthcare professionals (HCPs), patients, and stakeholders with tailored messaging. Heres how pharma brands can maximize impact: 1. Drug names and indications must align with FDA-approved labeling.

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Pharma Marketing Network

MARCH 3, 2025

Imagine launching a campaign that reaches the right doctor at the right time or helps a patient understand treatment options without feeling overwhelmed. Digital advertising campaigns allow pharmaceutical brands to connect with their audiences at critical moments in the healthcare journey.

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Pharma Marketing Network

MARCH 3, 2025

Imagine launching a campaign that reaches the right doctor at the right time or helps a patient understand treatment options without feeling overwhelmed. Digital advertising campaigns allow pharmaceutical brands to connect with their audiences at critical moments in the healthcare journey.

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pharmaphorum

FEBRUARY 18, 2021

Price decay after loss of brand exclusivity”. Focused and effective late lifecycle management can preserve meaningful value for the brand. Kellogg’s Corn Flakes had “generic” competition within a month of its launch more than 100 years ago, and yet it’s still the dominant brand in its market.

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Delveinsight

AUGUST 3, 2021

Nevro Received FDA Approval of its 10 kHz High-Frequency Spinal Cord Stimulation Therapy for Treatment of Chronic Pain Associated with Painful Diabetic Neuropathy. received approval for its Senza System, Nevro’s unique 10 kHz stimulation, to treat chronic pain associated with Painful Diabetic Neuropathy (PDN).

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XTalks

MARCH 16, 2022

The branded campaign includes a TV commercial (linked in the image above) that features Couric cooking dinner with her 30-year-old daughter Ellie as well as snippets of her conversations with people about their reasons for colon cancer screening. Exact Sciences is eyeing an FDA approval for a newer version of its test, Cologuard 2.0,

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The Pharma Data

JUNE 18, 2021

Today, the brand is launching ‘ See Yourself’ , a new campaign featuring documentary style shorts that dive deep into the stories of real BOTOX ® Cosmetic patients – people of all shapes, sizes, backgrounds, colors, and origins. IRVINE, Calif. BOTOX ® Cosmetic Important Information.

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pharmaphorum

FEBRUARY 2, 2021

However, as the pandemic took hold BMS opted to delay its launch, mindful that prescribing rates could be held back by the lack of patient contact with doctors. One key rival could be AbbVie’s JAK inhibitor Rinvoq (upadacitinib) which picked up an FDA approval for this indication last month to add to its current use in rheumatoid arthritis.

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Pharmacy Checkers

NOVEMBER 21, 2019

Eban’s greatest concern is with generic drugs, she hints at potential problems with brand name drugs as well, since the active pharmaceutical ingredients that go into all these medications are made in India and China, where manufacturing problems are greater, relative to the U.S. This is the heart of FDA’s mission. drug supply.

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The Pharma Data

JUNE 28, 2021

There are currently no FDA-approved anticoagulation therapies for pediatric patients with congenital heart disease who have undergone the Fontan procedure. About Rivaroxaban (Xarelto ) Rivaroxaban is the most broadly indicated non-vitamin K antagonist oral anticoagulant (NOAC) worldwide and is marketed under the brand name Xarelto.

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FDA Law Blog

JANUARY 26, 2022

I’ve leaned on all kinds of doctors and professionals for help” (Ryan Murphy TV Ad). In addition, because the ads referenced migraine, the ads should have included “material information regarding Emgality’s full FDA-approved indication,” notably, that Emgality is indicated for the preventive treatment of migraine in adults.

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Clinical Trial Podcast

FEBRUARY 23, 2021

Say you’re in the midst of securing FDA approval to start a new clinical trial. You find out that the FDA has follow-up questions. Or go to the doctor for an annual check-up? Lawsuits impact the company’s finances, brand and reputation. Let me give you an example. Interested in Key Performance Indicators (KPIs).

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STAT News

JULY 15, 2022

It was the weekend: his doctor wasn’t available, an emergency department provider told him he might have anal cancer, and an urgent care provider sent him home with Tylenol and no diagnosis. Andy couldn’t sleep more than a couple fitful hours a night because it felt like a hot fork was stabbing him in the butt.

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pharmaphorum

JANUARY 21, 2021

Bayer and Merck & Co’s heart failure drug vericiguat has been approved by the FDA under the brand name Verquvo, in an increasingly competitive market. Entresto (sacubitril+valsartan) was FDA-approved in patients with reduced ejection fraction five years ago.

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FDA Law Blog

AUGUST 21, 2023

Livornese — I saw the sign…and the answer is no—FDA-approved labeling apparently is not enough under state failure-to-warn laws, according to certain courts. Brand drugs, generic drugs, and medical devices alike have all been the target of state failure-to-warn litigation; in a recent case, OTC acetaminophen is the target.

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FDA Law Blog

MAY 11, 2023

Specifically, the Government explained, “[t]he section viii pathway cannot function properly if FDA and generic manufacturers cannot rely on an NDA holder’s representations to the agency regarding which portions of the brand-name drug’s labeling teach patented methods of use.”

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pharmaphorum

SEPTEMBER 30, 2022

Patient organisations have been celebrating the FDA approval yesterday of Amylyx’ amyotrophic lateral sclerosis (ALS) therapy Relyvrio, after not one but two advisory committee meetings that arrived at different conclusions about the drug.

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Intouch Solutions

AUGUST 5, 2021

For trans individuals, years may pass between doctor visits because of the emotional and financial tolls that can accompany them. Aside from being casually misgendered by office staff, she was eventually placed with a doctor that had working knowledge of trans needs, but even then, experienced hurdles.

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Intouch Solutions

JULY 31, 2022

The “nextmakers” of EVERSANA INTOUCH know the Medical Metaverse is changing everything, whether you’re a patient, provider, caregiver… or brand marketer. The video game prescribed by doctors (bbc.com). Here’s a bonus video from Siemens on the importance of digital twins. Digital therapeutics in focus.

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Eye on FDA

APRIL 15, 2020

Finally, they underscore the innovation of a company that is vital to its brand. Bristol Myers Squibb stated in its press release announcing FDA approval of the company’s treatment for multiple sclerosis that the commercial launch would be delayed due to the COVID-19 situation. Recently in the U.S.

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The Pharma Data

OCTOBER 23, 2020

Remdesivir gets full FDA approval to treat COVID. Remdesivir’s full approval Thursday by the FDA comes after the agency granted it emergency use authorization last spring. is selling the drug under the brand name Veklury. Doctors say this reflects India’s younger and leaner population.

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The Pharma Data

OCTOBER 24, 2020

Remdesivir gets full FDA approval to treat COVID-19. Remdesivir’s full approval Thursday by the U.S. is selling the drug under the brand name Veklury. Doctors say this reflects India’s younger and leaner population. It is given intravenously to hospitalized patients.

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The Pharma Data

MAY 13, 2021

WITHOUT doctors, physical therapists or chiropractors. Our Unique Solution Has Been Featured All Over The Media, From Hallmark, The Doctors, Atlanta Live & Arizona Midday…. I Have A Doctorate In Pharmacy, But Everything I Learned About Pain Relief In Pharmacy School Is Dead Wrong! And then got my Doctor of Pharmacy (Pharm.

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XTalks

DECEMBER 20, 2023

And this year Eli Lilly stepped into the obesity drug market with its own GLP-1 weight loss drug Zepbound (tirzepatide), which the US Food and Drug Administration (FDA) approved in November of this year. report indicating that they accounted for half of the most viewed new brands. billion ad impressions.

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Drug Patent Watch

JANUARY 7, 2025

Generic drugs are pharmaceutical products that contain the same active ingredients as their brand-name counterparts. They’re designed to be bioequivalent, meaning they have the same dosage, strength, route of administration, quality, and intended use as the original brand-name drug.

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Pharma Marketing Network

MARCH 5, 2025

With millions of healthcare professionals (HCPs) and patients turning to Google for medical information, paid search ads present a huge opportunity for pharma brands to boost engagement and conversions. Being present at the top of search results improves brand awareness. However, the landscape isnt simple.

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The Pharma Data

JUNE 18, 2021

IMBRUVICA is the only FDA-approved medicine in WM and cGVHD. IMBRUVICA was one of the first medicines to receive FDA approval via the Breakthrough Therapy Designation pathway. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. The full U.S.

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Pharma Marketing Network

MARCH 8, 2025

But in an industry with strict regulations, high competition, and complex audience needs , landing page optimization for pharmaceutical brands requires a strategic and compliant approach. It must convert visitors into leads , provide clear and accurate medical information , and ensure compliance with FDA, HIPAA, and ad platform policies.

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The Pharma Data

JUNE 18, 2021

IMBRUVICA is the only FDA-approved medicine in WM and cGVHD. IMBRUVICA was one of the first medicines to receive FDA approval via the Breakthrough Therapy Designation pathway. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. . The full U.S.

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World of DTC Marketing

JULY 27, 2021

COVID vaccines, already in use, have not received full FDA approval. Virtual doctor visits had been declining as I forecasted they would, but now they could climb again. SUMMARY: The CDC is recommending that vaccinated people wear masks again in some states. Every family physiican should be recommending COVID vaccinations.

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The Pharma Data

MAY 4, 2021

down 21%, driven by a negative impact from the COVID-19 pandemic resulting in a decline in patient visits to doctors for preventative health purposes, as well as the loss of patent protection in the U.S. Lorbrena is now indicated for adults with metastatic NSCLC whose tumors are ALK-positive as detected by an FDA-approved test.

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XTalks

JANUARY 31, 2025

The ad then switches gears from doom and gloom to hope that providers like Hims & Hers promise to bring through life-changing weight loss medications, which are affordable, doctor-trusted and formulated in the USA. In contrast, Hims & Hers introduced compounded semaglutide injections last May starting at $199 per month.

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The Pharma Data

OCTOBER 27, 2020

Remdesivir gets full FDA approval to treat COVID-19. The antiviral drug remdesivir has received full approval from the U.S. The approval comes after the agency granted it emergency use authorization last spring. The approval comes after the agency granted it emergency use authorization last spring.

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