PM360

OCTOBER 28, 2022

First, as every pharma marketer knows, Medical Legal Regulatory (MLR) review and approval is a legal layer of consumer protection, confidence, and clarity. In addition, content platforms enable automated and streamlined management of asset metadata, tagging, usage tracking, and searchability.

Marketing 98

Marketing Pharma Consulting Management 98

PM360

JUNE 26, 2023

In commercial, issues related to Medical, Legal, and Regulatory (MLR) review compliance will need to be carefully managed as well. Auto-tagging, a laborious task, is another area where generative AI/LLMs can assist. Auto-tagging helps the right content get delivered to the appropriate customers.

Pharma 97

Pharma Management Ethics Medical science 97

PM360

OCTOBER 13, 2023

While marketing teams and Medical/Legal/Regulatory (MLR) reviews will still be necessary for refining this content, AI can significantly expedite the content creation process and empower marketing teams to work more efficiently. Another capability made possible by fine-tuning is the enhancement of content tagging.

Marketing 64

Marketing Specialization Healthcare Healthcare 64

World of DTC Marketing

JUNE 23, 2021

The story of how a drug that’s never even been proven to work is now poised to rake in billions of dollars for its manufacturer, impose needless suffering on millions of families, and destabilize Medicare and Medicaid in the process, goes well beyond the failures of what should be the toughest regulatory body of the U.S. government.

FDA 218

FDA Side effects Physicians Patients 218

pharmaphorum

AUGUST 25, 2022

Johnson & Johnson has its first worldwide regulatory approval – in the EU – for Tecvayli, one of two much-anticipated bispecific antibodies the drugmaker has developed for patients with multiple myeloma. Tecvayli previously scored a priority medicines (PRiME) designation from the EMA and a breakthrough-therapy tag from the FDA.

FDA 93

FDA Marketing Safety Patients 93

Pharmaceutical Technology

NOVEMBER 9, 2022

million price tag. While experts interviewed by Pharmaceutical Technology found the cost-effectiveness estimates valid, the durability of gene therapies in haemophilia remains unclear, particularly in the case of Roctavian, which has faced similar queries from regulatory authorities. appeared first on Pharmaceutical Technology.

Safety 111

Safety Pharmaceutical Patients Medicine 111

pharmaphorum

AUGUST 21, 2022

There’s no word yet on its pricing, but for comparison Spravato was launched with an annual price tag of around $32,400, which the Institute for Clinical and Economic Review (ICER) concluded was around 25% to 52% too high to be cost effective.

FDA 88

FDA Marketing Pharma Sales 88

pharmaphorum

JULY 25, 2022

Tecvayli previously scored a priority medicines (PRiME) designation from the EMA and a breakthrough-therapy tag from the FDA. after a median follow-up of just under four months, and Pfizer is looking at potential regulatory filings later this year. In the MagnetisMM-3 trial, elranatamab was associated with an ORR of 60.6%

Medicine 52

Medicine FDA Recruitment Patients 52

Pharmaceutical Technology

MAY 2, 2023

Chimeric antigen receptor T-cell (CAR-T) therapies are the only genetically modified cell therapies to have received regulatory approval, and they are currently utilised in relapsed/refractory settings. Cost-related unmet needs also scored highly.

Physicians 52

Physicians Marketing Patients Manufacturing 52

Vodori

AUGUST 10, 2022

For example, if your regulatory team offers feedback on a marketing-focused element like an image or color choice, consider this as a suggestion. If feedback is provided outside your area of expertise, tag all appropriate departments for their input.

Marketing 52

Marketing Healthcare Healthcare 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.

Food and Drug Administration 105

Food and Drug Administration Electronics Pharma FDA 105

Contrarian Sales Techniques

JANUARY 23, 2024

The map leads you through regulatory landscapes, navigating intricate FDA and compliance guidelines. Some found the material dense, the exam daunting, and the price tag a tad hefty. It delves into the science behind the drugs, equipping you with knowledge of anatomy, physiology, and therapeutic areas. But here's the thing.

Pharmaceutical Sales 52

Pharmaceutical Sales Pharmaceutical Sales Ethics 52

Salesforce

DECEMBER 18, 2023

Here’s how it can help you effectively manage your assets and some benefits you’ll achieve: Enhanced asset visibility and tracking: Technologies like IoT, RFID tags, barcodes, and GPS help you monitor the location and status of your assets in real time by communicating to your field service management.

Management 59

Management Safety Manufacturing Retail 59

pharmaphorum

NOVEMBER 16, 2022

However, with a price tag of €1.58 However, a recently released report from the organisation could blow the price tag of Zolgensma out of the water. When even high-income regions like Europe are refusing to meet the price tag of certain gene therapies, it is likely the debate on pricing is set to continue in the long-term.

Medicine 124

Medicine Marketing Healthcare Healthcare 124

Contrarian Sales Techniques

DECEMBER 4, 2023

Personalize with Name Tags or Initials: A Personal Touch Adding a name tag or your initials can give your sample bag a personal touch. Complying with Regulations: A Legal Mandate First and foremost, the distribution of pharmaceutical samples is subject to stringent regulatory requirements.

Sales 52

Sales Pharmaceutical Sales Pharma Ethics 52

Rep-Lite

MARCH 21, 2024

It’s important to note, however, that products that are subject to stringent regulatory requirements may require more extensive training and compliance efforts which can then also be reflected in their earning capacity. There are rungs and each comes with both a price tag and an incentive.

Medical sales 52

Medical sales Medical sales reps Medical Sales 52

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. Over the years, pharmaceutical companies seeking product approvals have submitted increasingly vast amounts of information to regulatory agencies.

Management 52

Management Pharmaceutical Marketing Electronics 52

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 the limited market, the price tags of haemophilia make it potentially lucrative. Haemophilia B is a rare condition.

Patients 98

Patients Food and Drug Administration Engineering Sales 98

European Pharmaceutical Review

JULY 11, 2022

Funding of up to $30 million will support vaccine design, its development through Phase I trials and regulatory activities. . These coronavirus RBDs are attached to a nanoparticle by protein tags, enabling the structure to display fragments from multiple viruses on a single nanoparticle. . The innovative protein ?“glue”

Manufacturing 96

Manufacturing Engineering Leads Medicine 96

pharmaphorum

OCTOBER 4, 2022

The eConsent platform is a regulatory-compliant electronic consent system for clinical trials and the Rave EDC is a secure system for clinical trial site, patient, and lab data capture and management. Medidata has provided its Patient Cloud and Rave solutions to the Biobank, which includes eConsent and Rave EDC (electronic data capture).

Electronics 93

Electronics Patients Management Insurance 93

Cadensee

JANUARY 1, 2022

A lot of regulatory multiple add-ons, a lot of issues related to mass production and manufacturing is very easy. It's already tagged by clinicians with the diagnosis, so you have to do the machine learning and the engineering side. So, the difficulty is really behind the scene. Consumers are getting it in a very simple way.

Marketing 52

Marketing Physicians Medical Healthcare 52

European Pharmaceutical Review

DECEMBER 27, 2023

This is in addition to its considerable price tag. The demand for CAR T-cell therapy is therefore much greater than the supply, making it difficult for patients to access the potentially life-saving treatment. These criteria may put constraints on smaller facilities and make it unfeasible.

Manufacturing 88

Manufacturing Food and Drug Administration Patients Pharma 88

Pharmaceutical Technology

NOVEMBER 30, 2022

The company’s weight loss drug Saxenda (liraglutide) won an approval for chronic weight management in December 2014, and Wegovy (semaglude) got the same tag in 2021. We highlight the most impactful emerging technologies, as well as the industry, regulatory, and macroeconomic factors that influence growth prospects. compared to a 5.1%

Medical 105

Medical Manufacturing Insurance Side effects 105

Pharmaceutical Technology

NOVEMBER 30, 2022

The company’s weight loss drug Saxenda (liraglutide) won an approval for chronic weight management in December 2014, and Wegovy (semaglude) got the same tag in 2021. We highlight the most impactful emerging technologies, as well as the industry, regulatory, and macroeconomic factors that influence growth prospects. compared to a 5.1%

Medical 98

Medical Manufacturing Insurance Side effects 98