PharmaKinnex

AUGUST 23, 2022

The Traditional Pharma Model Isn’t Working – It’s Time to Evolve! From new legislation to functional shifts in marketing and advertising, the pharma industry works hard every day to keep up with new regulatory requirements and the constantly evolving expectations of prescribers and patients. More convenience and safety?

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European Pharmaceutical Review

APRIL 2, 2024

At Roche, we see it as our ethical and environmental responsibility to support the use of alternative methods that prioritise animal welfare while ensuring the safety of our patients and the quality of our products. These methods aim to impede animal suffering by reducing dependence on horseshoe crab blood.

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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. appeared first on Pharma Marketing Network.

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pharmaphorum

OCTOBER 14, 2022

A consortium of industry and academic groups – led by Johnson & Johnson’s pharma division Janssen – has been set up to tackle the environmental impact of digital health products, specifically aimed at minimising waste that could end up in landfill. Photo by Possessed Photography on Unsplash.

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Pharmaceutical Technology

JUNE 15, 2023

With the power of AI, healthcare organizations are streamlining pharma R&D , revolutionizing patient care and improving business operations. Developing safe and effective drugs Pharma researchers are using AI in the earliest stages. AI’s ability to analyze data quickly also contributes to safety, including during clinical trials.

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Pharma Marketing Network

MAY 15, 2023

Additionally, by analyzing data from completed clinical trials, companies can gain insights into the safety and effectiveness of their products, which can inform the development of new drugs. Additionally, companies must ensure that the data they collect is accurate and reliable, and that it is used ethically and responsibly.

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Pharma Marketing Network

MARCH 23, 2023

Additionally, by analyzing data from completed clinical trials, companies can gain insights into the safety and effectiveness of their products, which can inform the development of new drugs. Additionally, companies must ensure that the data they collect is accurate and reliable, and that it is used ethically and responsibly.

Pharmaceutical 52

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Clarivate

NOVEMBER 13, 2023

The purpose of clinical trials is to understand the efficacy and safety of treatments for the patients who need them. We developed or explored over 100 COAs and achieved ethical approval in multiple countries including the U.S., Mainland China and Japan.

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Contrarian Sales Techniques

JANUARY 27, 2023

It can be challenging when you find yourself promoting products that seem to contradict each other, as it can raise questions about the effectiveness and safety of the products you're selling.

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MedReps

SEPTEMBER 19, 2022

There’s no shortage of challenges for those new to pharma, medical sales and even veterans. First, they’ll likely have more interest in learning about what you sell and second, they’ll be more hesitant to try it because of concerns about insurance coverage, efficacy and safety. Competitors and Generic Medications.

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Medical sales Medical sales reps Medical Sales 66

pharmaphorum

NOVEMBER 16, 2022

So, really,” he continued, “[there are] three major take-homes to talk about: first efficacy, then function, and then safety. Additionally,] in my opinion probably the most important safety angle to consider is rates of wet AMD [age-related macular degeneration] were increased with pegcetacoplan treatment, that is 12.2%, 6.7%, and 3.1%

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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. Patients want to know other patients are involved in what pharma is doing. Learn how pharma is involving them. They want to hear about those patients’ experiences.

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Patients Pharma Education Media 59

European Pharmaceutical Review

MAY 2, 2023

By collaborating with several stakeholders and authorities, multiple stages of development can take place concurrently to speed up R&D without compromising safety protocols. Available from: [link] Pharma R&D return on investment falls in post-pandemic market [Internet]. The COVID-19 blueprint has shown a way forward.

Patients 101

Patients Medicine Marketing Medical 101

pharmaphorum

NOVEMBER 3, 2022

We see how digital measures of adherence ensure that sample size calculations hold and drug developers can accurately evaluate the safety and efficacy of new molecules. Pharma companies with more mature digital strategies are able to focus on questions of scale. The post How pharma can thrive in the digital era appeared first on.

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Clarivate

MARCH 17, 2022

How feasible is it to establish a drug’s safety for use in a population that may be unwilling or unable to participate in clinical trials? Margolis Center for Health Policy to convene a February 2021 public meeting about scientific and ethical issues associated with enrolling pregnant individuals in clinical trials for drug development.

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Pharmaceutical Technology

DECEMBER 21, 2022

This is true not only in the case of the general public using applications for creating images or text, but also for pharma companies to improve drug discovery, clinical trial recruitment, and finding new biomarkers. Across all sectors, AI applications are being used to increase efficiency and reduce costs. Canada makes moves for privacy.

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Pharma Medicine Pharmaceutical Government 140

Clarify Health

DECEMBER 13, 2022

About 10% of pharma companies at this point have active efforts but we’ve started to see some approvals. And, as you get into more specialty and rare conditions, the need from a cost, ethical, and frankly just a workflow perspective is only going to increase,” Mr. Clapsis added. It’s not just the FDA,” he said.

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Clarify Health

DECEMBER 13, 2022

About 10% of pharma companies at this point have active efforts but we’ve started to see some approvals. And, as you get into more specialty and rare conditions, the need from a cost, ethical, and frankly just a workflow perspective is only going to increase,” Mr. Clapsis added. It’s not just the FDA,” he said.

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Recruitment Retail Patients Education 52

Pharmaceutical Technology

MARCH 16, 2023

However, health specialists refute most safety concerns for the use of drug classes as part of gender affirming care, citing years of research and care. One of the reasons why organisations, including pharma companies, do not enter this debate is because these drugs are used off label, says Horowicz.

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