pharmaphorum

JANUARY 27, 2023

Having previously spoken with Dr Mullen three years ago when she was country medical director for the UK & Ireland at GSK – on the topic of patient centricity and embedding that focus within the core of a pharmaceutical company – our recent interview provided some interesting insights into the changing landscape of the industry.

Patients 94

Patients Pharmaceutical Medical Physicians 94

World of DTC Marketing

JANUARY 8, 2021

At the time, pharmaceutical giant Pfizer and its partner BioNTech—which now have the other US-authorized COVID-19 vaccine—had inked a deal with the US government to supply doses at $19.50 Also, Johnson & Johnson had a deal to supply the US government with doses of its vaccine—still in the works—at a rate of $10 per dose.

Government 266

Government Safety FDA Pharma 266

Pharmaceutical Technology

OCTOBER 17, 2022

The UK Government has announced funding worth more than $894.6m (£800m) to back research into ground-breaking, experimental therapies and progress the response of the country to patient safety challenges. These research centres comprise a new facility in Exeter.

Safety 52

Safety Government Competition Patients 52

pharmaphorum

JANUARY 16, 2023

. “Although the totality of the data currently suggests that it is very unlikely that the signal…represents a true clinical risk, we believe it is important to share this information with the public, as we have in the past, when one of our safety monitoring systems detects a signal,” said the statement. 1 variant of Omicron.

Safety 103

Safety Government FDA Patients 103

World of DTC Marketing

JULY 21, 2021

Here are some myths around DTC marketing: 1ne: DTC ads result in patients asking for prescriptions they don’t need. 3hree: DTC marketing minimizes the side effects of prescription drugs – One of the top pages within prescription drug websites continues to be “safety information.”

Marketing 285

Marketing Prescription Side effects Doctors 285

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.

Insurance 98

Insurance Government Safety Patients 98

Legacy MEDSearch

JULY 21, 2023

UroMems , a global company developing innovative, mechatronics technology to treat stress urinary incontinence (SUI), announced today that it has successfully completed the first-ever implant of the UroActive smart, automated artificial urinary sphincter (AUS) in a female patient. Food and Drug Administration).

Food and Drug Administration 52

Food and Drug Administration Patients Safety Recruitment 52

World of DTC Marketing

APRIL 15, 2021

While patients have the right to full disclosure, misinformation and scare tactics could lead to more deaths from COVID. Also cited was a lack of trust in the government to ensure the vaccines’ safety and effectiveness. The government allowed the drugmakers to mass-produce the vaccine while still conducting clinical trials.

Food and Drug Administration 203

Food and Drug Administration Government Safety Side effects 203

World of DTC Marketing

OCTOBER 20, 2020

There has to be a complete investigation as to why the patient suffered ill effects including the possibility that he/she had a known or unknown health condition. “It’s troubling, to say the least, and I can’t recommend any vaccine to a patient until I know a hell of a lot more,” said one physician I talked to.

Pharma 214

Pharma Government Physicians Safety 214

pharmaphorum

OCTOBER 26, 2022

And just as a family business thrives on its connection to the community, Chiesi is committed to connecting to the global patient community. We try to have a very long-term orientation because we believe that aligns our objectives very well with the objectives of society and the patients we serve, and it makes us a stable business.”.

Patients 76

Patients Pharma Consulting Transportation 76

Nixon Gwilt Law

APRIL 22, 2024

Its three separate Rules (Security, Privacy, and Breach) impose a variety of security controls, documentation, governance, and notice requirements on custodians of protected health information (PHI). The HTI-1 Final Rule is an AI disclosure and governance rule published by the US Department of Health and Human Services (HHS).

Healthcare 52

Healthcare Healthcare Training Food and Drug Administration 52

PM360

OCTOBER 28, 2022

With this in mind, in order to maximize the benefits of AI while mitigating its related risks, pharmaceutical incumbents and startups need to implement AI governance processes and tools. Likewise, it enables them to predict the effect of the compound on the target and the compound’s safety risks. Promising AI Use Cases in Pharma.

Pharma 105

Pharma Food and Drug Administration Government Medicine 105

Pharmaceutical Technology

NOVEMBER 22, 2022

Additionally, a contract with the ministry for the Japanese government to procure one million courses of Xocova has become effective with the approval. The latest development is based on the expected efficacy of the drug and the acceptability of its safety profile reported from a Phase II/III clinical trial.

Government 98

Government Safety Pharmaceutical Manufacturing 98

Pharmaceutical Technology

JULY 7, 2022

The two non-competing SARS-CoV-2 monoclonal neutralising antibodies, amubarvimab and romlusevimab are obtained from convalesced Covid-19 patients. The treatment is indicated for such patients who are at increased risk for disease progression, including hospital admission or mortality. 2 subvariants.

Food and Drug Administration 105

Food and Drug Administration Distribution Government Food 105

Celeritas

SEPTEMBER 26, 2022

A) Aiding Healthcare Professionals (HCPs): Storage of Patient Information: The common method of use of QR codes is in the organization and accessibility of patient records. In essence, patients’ files are all synced to a medical database. They’re ideal for monitoring elderly patients who tend to wander off or sleepwalk.

Physicians 52

Physicians Patients Medical Management 52

PM360

JUNE 11, 2022

Only 5% of patients ranked pharma companies as the most trusted player in the healthcare space, according to a 2021 survey of 500 patients from Accenture. But 71% also want publicly shared information about how patients’ perspectives were incorporated into the development of products and services. Noël Moossa.

Patients 59

Patients Pharma Education Media 59

European Pharmaceutical Review

NOVEMBER 20, 2023

“This state-of-the-art parenteral site with the latest technology will enable us to continue to deliver medicines with safety first and quality always around the world,” stated Edgardo Hernandez, Executive Vice President and President of Eli Lilly’s manufacturing operations.

Manufacturing 82

Manufacturing Medicine Biopharma Engineering 82

European Pharmaceutical Review

JUNE 16, 2023

The authors argued that fundamentally, implementation of AI/ML for pharmacovigilance has been hindered by the associated legal framework processes and governance issues. concluded: “If we do not harness the properties of data to allow us to leverage AI optimally, we will fail to do all we can for patient safety.” Bate et al.

Safety 88

Safety Electronics Medicine Government 88

European Pharmaceutical Review

NOVEMBER 15, 2022

According to IGBA, the World Health Organization ( WHO) Biosimilars Guideline has been a useful tool for health authorities to boost international regulatory convergence and consistency of terminology when evaluating biosimilars, by approving quality, safe and efficacious biosimilar medicines for patients who otherwise would have lacked access.

Medicine 89

Medicine Safety Healthcare Healthcare 89

PM360

JUNE 26, 2023

This includes ensuring access and affordability of their products, which can positively impact their environmental social governance (ESG) score and reputation. These partnerships can be with local governments, healthcare providers, local startups, and non-governmental organizations. In a shareholder meeting, Merck & Co.

Medicine 98

Medicine Marketing Pharma Manufacturing 98

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. Mainland China has taken significant steps toward improving access to treatment for its estimated 20 million rare disease patients in recent years. [1]

Patients 52

Patients Food and Drug Administration Marketing Pharma 52

European Pharmaceutical Review

OCTOBER 1, 2022

In order to carry out this work, the Council stated that governments must know which patient populations require supply and have accurate tissue and cell availability data to action this. Improving communication between public health authorities was also a key aim.

Ethics 90

Ethics Distribution Government Safety 90

World of DTC Marketing

AUGUST 20, 2020

It’s estimated that between 30-40% of people won’t get the vaccine because they either don’t believe in vaccines or they have lost trust in our government to approve a safe and effective vaccine. Polls show that as the pandemic has continued, US citizens have become less confident about the safety of a vaccine.

Media 249

Media Pharma Government Consulting 249

European Pharmaceutical Review

DECEMBER 21, 2022

The Dutch government offers a prime example. Despite the tidal wave of renewed interest in psychedelic therapies, there is still much to be learned about them, including their precise mechanisms of action, their long- and short-term safety profiles, the durability of their effect, and their adverse effects—which can be severe.

Food and Drug Administration 106

Food and Drug Administration Medicine Food Government 106

Pharma Marketing Network

JULY 26, 2023

As new healthcare challenges arise and the pharmaceutical landscape evolves, the FDA may be allocating its resources to focus on other pressing issues, such as drug approvals, monitoring emerging health threats, and enhancing drug safety.

Marketing 97

Marketing FDA Food and Drug Administration Pharmaceutical 97

Pharmaceutical Technology

MAY 25, 2023

The Medicines and Healthcare products Regulatory Agency (MHRA) aims to launch a pilot genetic biobank that will gather patient data to associate drug-related adverse events to their genetic makeup. The Yellow Card biobank will launch as a joint venture with the UK-government funded entity Genomics England on June 1.

Side effects 52

Side effects Medicine Recruitment Doctors 52

Contrarian Sales Techniques

FEBRUARY 25, 2023

The film documents the efforts of activists, doctors, and patients to overcome these barriers and increase access to affordable treatment. This can result in shortages of certain medications, which can have serious consequences for patients who depend on those medications for their health.

Marketing 52

Marketing Distribution Medical Government 52

Pharma Marketing Network

JANUARY 6, 2021

Tools that help people track their health, including apps, wearables, and patient portals will be used more than ever in 2021. Due to the pandemic, the healthcare industry has gone almost completely virtual Patient visits with HCPs, meetings between HCPs and sales reps, and healthcare conferences have all had to endure the virtual shift.

Marketing 98

Marketing Pharma Media Safety 98

pharmaphorum

NOVEMBER 3, 2022

The two phase 3 studies – called EAGLE-2 and 3 – were stopped early by their data monitoring committees after an interim look at the data showed clear efficacy and safety for GSK’s drug. There are real concerns that we could be entering a post-antibiotic era, where even minor infections can be enough to kill patients.

Pharma 97

Pharma Government Patients Safety 97

Pharmaceutical Technology

DECEMBER 22, 2022

Theft, fraudulent prescriptions and unsanctioned distribution by patients and medical practitioners are the most common ways in which legal fentanyl products are illegally secured. Increased trafficking of illegal fentanyl represents a new threat to public health and safety. A lethal drug that creates its own demand.

Safety 105

Safety Manufacturing Distribution Prescription 105

Pharmaceutical Technology

MARCH 23, 2023

These changes come following a public consultation with the Healthcare Research Authority, to which a government response was published on March 21. The agency reports that, in the pilot phase, these revisions halved the approval times for studies and cut the time from application to recruiting the first patient by 40 days.

Healthcare 59

Healthcare Healthcare Recruitment Government 59

Pharmaceutical Technology

JUNE 8, 2023

The core objective of the collaboration is to make the therapies affordable and accessible to patients. The companies will offer a comprehensive suite of cell therapy services to biotech, pharmaceutical and government entities, and to hospitals. Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva.

Manufacturing 52

Manufacturing Government Safety Pharmaceutical 52

pharmaphorum

NOVEMBER 24, 2022

The opportunity is open to academic, government, and industry organisations anywhere in the world, with a lead partner based in the UK. Dr Catherine Kettleborough, lead of the LifeArc Chronic Respiratory Infection Translational Challenge, said: “Repurposing an existing drug or compound is a faster way of getting new treatments to patients.

Government 57

Government Leads Safety Medical 57

Contrarian Sales Techniques

FEBRUARY 24, 2023

In the blog post here , I’ve shared several tips to help patients cut down on costs, such as buying generic medications, shopping around for the best prices, and taking advantage of discounts and promotions offered by pharmacies. What is the hospital's patient-to-nurse ratio? What are the hospital's patient satisfaction rates?

Medicine 52

Medicine Healthcare Healthcare Insurance 52

European Pharmaceutical Review

AUGUST 23, 2022

FAKE MEDICINES are not a new problem, and pose a tremendous threat to patient safety and public health in society regardless of a country’s economic status. Unfortunately, such a chain of custody is not intended to provide patients with the ability to verify their own medicines. About the author.

Medicine 90

Medicine Food and Drug Administration Pharmaceutical products Pharmaceutical 90

Pharmaceutical Technology

JULY 25, 2022

Digitalization is now in full swing as medical care integrates with ICT to take the patient experience to the next level. There are already opportunities for patients to track their health through smart medical devices sending reports directly to their healthcare provider.

Pharmaceutical 114

Pharmaceutical Engineering Healthcare Provider Healthcare 114

Clarity Engagement Solutions

NOVEMBER 9, 2020

The process of approval was simple: once the data showed the efficacy, safety and reliability to the regulatory agencies, the drug was approved. The goal is to create a collaborative relationship with stakeholders based around the development of the value propositions that address the needs of policy makers, patients and payers.

Marketing 91

Marketing Key account management Pharma Prescription 91