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Exceeding Budgets & Falling Short: EVERSANA Leaders Tell Hard Truths About Omnichannel

Eversana Intouch

Are more prescriptions being written and fulfilled to validate the time, money, and resoures allocated? Are those ‘seamless brand experiences’ integrating the right mix of digital tools and one-on-one personal engagements actually accelerating patients’ time to therapy and delivering business impact?

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FDA tackles opioid crisis with OTC Narcan approval

Pharmaceutical Technology

The overdose death rate in the US increased more than 250% from 1999 to 2019, as per a Canada-US joint white paper on substance use and harms. Between 1999 and 2021, overdose deaths from synthetic opioids excluding methadone increased 97-fold, and prescription opioid overdose deaths increased 4.9-fold,

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It’s time get real with healthcare’s commitment to net zero

pharmaphorum

A study of public tenders for prescription medicines between 2014 and 2019 shows a fall in multi-criteria tenders rewarding “environmental” attributes and an average weighting of only 5% (see Figure 2). Where tenders are concerned, greater weight should be given to sustainable criteria, which is well understood, but poorly implemented.

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Quality by design with a focus on biosimilars

Pharmaceutical Technology

For more information on this, please download our white paper. For more information, please download our white paper. Regardless of whether a drug product is intended for mass populations or certain prescriptions, QbD should always be followed in its development. “In

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Pharma’s post-pandemic launch performance problem: what’s the prognosis?

pharmaphorum

The prescription medicine market has recovered from the wild swings of the early pandemic with renewed growth. Non-COVID prescription medicines didn’t stop launching during the pandemic — approvals by both the FDA and the EMA were, in fact historically high in both 2020 and 2021. The scope of the problem.

Doctors 57
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Race to the finish: pharma edges closer to approval with RSV vaccines

Pharmaceutical Technology

Currently, GSK’s GSK 3844766A (RSVPreF3 OA) and Pfizer’s vaccine candidate RSVpreF (PF-06928316) may reach FDA approval first, having Prescription Drug User Fee Act (PDUFA) dates of May 3 and May 31, respectively. In a Phase III trial, GSK’s vaccine demonstrated a 94.1% reduction in severe RSV disease and overall vaccine efficacy of 82.6%.

Pharma 64
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Changing Health Care With AI-Assisted Robotic Devices With Charles Gellman

Evolve Your Success

We have a fantastic white paper for any of your readers at HidoHealth.com. A lot of the relationships that we are growing and communicating to are often the executive leaders that are able to read a white paper or maybe they don’t come across a video. We have an 80% reduction over 12 months. You can jump in there.