Express Pharma

JANUARY 12, 2024

Initiatives such as Ayushmaan Bharat Digital Mission (“ADBDM”), CoWIN (a digital vaccine delivery platform), health registry, and telemedicine, highlight the government’s strong emphasis on digitisation of health in India. For pharma and medical devices policies, the Department of Pharmaceutical is the nodal agency. –

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Pharmaceutical Technology

JUNE 16, 2025

These platforms are designed for safe drug production while allowing scaleable manufacturing processes. mRNA vaccine coverage on Pharmaceutical Technology (or Clinical Trials Arena) is supported by Trilink. The trial data indicated dose-dependent protein production at the site without systemic bioavailability. “By

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Putting Patients First Blog

APRIL 29, 2024

Communication and Transparency Clear Communication : We emphasize the need for documents to clearly and effectively communicate the nuances of the MPPP to beneficiaries, aiding in their decision-making process.

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pharmaphorum

JULY 19, 2021

Now, as vaccination continues at pace, the sector has pledged to help “build back better”, by lowering barriers between medical innovations and the patients who need them. As this report demonstrates, the biopharmaceutical indusyry is ready and willing to play its part in this process. Read the full report here. About the author.

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Express Pharma

MAY 7, 2024

Biogenerics comes with higher risks, as the manufacturing process and technologies are more complex. There is also a nod to India’s vaccine dominance which came to prominence during the global COVID pandemic. The DoP report also points out that biogenerics need different approaches to deal with IP challenges.

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Community Pharmacy

NOVEMBER 15, 2022

If this applies to you, then you can begin your application process here to get the process started. Medicare Part D has four phases of coverage that users need to be aware of before and during enrollment in the program. In 2022, the initial coverage limit was $4,430. In 2022, the coverage gap limit was $7,050.

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Putting Patients First Blog

JUNE 11, 2025

Its continuity and expertise are essential to ensuring that vaccine recommendations are based on the best available science-based evidence. Vaccination schedules must be grounded in scientific evidence, developed transparently, and implemented consistently.

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The Happy PharmD

SEPTEMBER 15, 2024

Or perhaps it’s the constant back-and-forth with insurance companies over coverage? This could be attributed to various factors, including the stage of career development and the process of finding professional fulfillment. Share your thoughts down below! Feel free to check it out!

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Pharmaceutical Commerce

JUNE 17, 2025

This is especially critical for temperature-sensitive biologics and vaccines, where maintaining proper storage conditions ensures product viability and regulatory compliance. Enhanced, continuous supply chain visibility is one of the most important elements of a safe, intelligent medication ecosystem.

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Pharmaceutical Technology

JUNE 20, 2025

Unlike vaccines, the agency leaders see the modality as a path to prevent and cure disease – aligning with the current administration’s wider national health strategy. Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva. Topic sponsors are not involved in the creation of editorial content.

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Pharmaceutical Technology

JUNE 16, 2025

Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva. Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content. Give your business an edge with our leading industry insights.

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Putting Patients First Blog

MARCH 29, 2023

They primarily focus on improving the public health infrastructure, improving the development of treatment and vaccines, and coordinating federal response. These flexibilities and partnerships greatly increased the speed of research and development for COVID-19 testing, treatment, and vaccines.

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Pharmaceutical Technology

JUNE 13, 2025

Robert Barrie June 13, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook mRESVIA is the second approved product in the US for Moderna, along with its Covid-19 vaccine Spikevax. Until now, the vaccine was licensed for the prevention of lower respiratory tract disease (LRTD) caused by RSV in adults aged 60 years and older.

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Putting Patients First Blog

SEPTEMBER 9, 2024

As these technologies become increasingly integral to patient care, it is essential for CMS to develop clear and consistent guidelines for the payment and coverage of AI-enabled services. Providing clear guidance, technical assistance, and streamlined processes can help facilitate the adoption of this innovative care model.

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Express Pharma

FEBRUARY 1, 2025

Sanjiv Navangul, MD & CEO, Bharat Serums and Vaccines The Union Budget 2025 reinforces India’s commitment to innovation, healthcare accessibility, and womens empowerment. The recommendation to allow up to 100 per cent FDI in insurance can be a complementary to the focus on enhancing access to cancer care.

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Pharmaceutical Technology

JUNE 10, 2025

Robert Barrie and Ross Law June 10, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook The removal ACIP members marks the most significant upheaval to the current vaccine landscape under Trump’s administration. lev radin via Shutterstock. lev radin via Shutterstock. Data Insights The gold standard of business intelligence.

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Pharmacy Times

JUNE 16, 2025

The first one was introduced on September 13, 2020, near the end of Trump’s first term, but was shut down by a federal judge due to the administration’s failure to comply with the proper implementation processes. Second, it does not address the core issues of higher prices, such as the use of rebates by insurers.

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