Remove Headlines Drug-Delivery
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Turning the TIDE: oligonucleotide development trends

European Pharmaceutical Review

Oligonucleotide therapeutics represent a relatively novel class of drug, with the potential to modulate drug targets that were previously considered intractable, and with the benefit of fast clinical development times. Small interfering RNA (siRNA) were one of the most preferred drug delivery methods. The answers?

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EMA unveils first projects as data partners join DARWIN EU project

pharmaphorum

Two years ago, the EMA proposed a set of recommendations to unlock the potential of big data for public health, headlined by the creation of a platform to access and analyse healthcare data from across the bloc. With the first data partners on board, the regulator can now move ahead with the start of its first studies.

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The criticality of compliance

pharmaphorum

Prior to selling drugs or medical products in any country, pharmaceutical companies must prove compliance and gain the regulatory approval required by the country in which the goods will be distributed in. In fact, the FDA cited data as the cause of 79% of Drug Warning Letters over the last five years.

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5 ways digital health, and digital pharma, changed in 2020

pharmaphorum

The rapid digitalisation of life during COVID-19’s acute phase also had a huge impact on healthcare delivery. The year began with Exscientia moving the world’s first AI-created drug into clinical trials in January and there were also signs of the technology’s potential in drug pricing and spotting COVID-19 in chest x-rays.

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Standards support medicines supply chain resilience and the future of quality

Quality Matters

While drug makers rely on USP standards for the clarity they provide on product quality specifications, regulators also look for manufacturer adherence to USP standards to indicate no additional validation of quality testing methods may be needed. In fact, USP documentary standards are recognized in U.S.

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Haven: The strategy that didn’t fix healthcare

pharmaphorum

At JP Morgan’s annual health care conference in January 2018, Dimon hosted a private dinner for about 25 top executives from pharmaceutical companies and advocated for lower drug prices. He told his guests, “We are not happy with healthcare costs and want to help.” Costs Remain a Problem.’. Cost” is not the problem.

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NHC Comments on Advance Notice of Methodological Changes for Calendar Year (CY) 2025 for Medicare Advantage (MA) Capitation Rates and Part C and Part D Payment Policies

Putting Patients First Blog

The CGDP has played a crucial role in helping to alleviate the financial burden on Medicare beneficiaries by reducing out-of-pocket (OOP) costs for prescription drugs. Part D Risk Sharing The NHC recognizes CMS’ ongoing efforts in risk sharing to mitigate financial risks faced by Part D sponsors due to unforeseen drug expenses.