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The 17th edition of CPHI & PMEC India, organised by Informa Markets in India, returns in an advanced format, scheduled from November 26-28, 2024, at the India Expo Centre, Greater Noida, Delhi-NCR. India’s pharma industry is on an impressive growth trajectory, expected to reach $65 billion by 2024 and to double to $130 billion by 2030.
What are the top 3 trends that defined pharma manufacturing in India and globally in 2024? In 2024, the pharmaceuticalmanufacturing landscape underwent transformative changes, driven by technological innovations, regulatory adaptations, and evolving global demands. and Europe. and Europe.
Integrating IT with pharmaceuticals will further strengthen its role, paving the way for dominance in biologics and biosimilars. The day concluded with the prestigious India Pharma Awards 2024, celebrating outstanding achievements in innovation and excellence within the pharmaceutical industry. With exports nearing $27.84
On Dec 24, 2024, Bio-Thera Solutions Inc. announced that it has partnered with Tabuk PharmaceuticalManufacturing Company to commercialize BAT2206, a proposed ustekinumab biosimilar to Jansen’s STELARA, in Saudi Arabia. Also on December 24, 2024, GlycoNex, Inc.
The 17th edition of CPHI & PMEC India, organised by Informa Markets in India, will take place from 26th to 28th November 2024 at the India Expo Centre, Greater Noida, Delhi-NCR. The event will showcase developments in pharmaceutical modernisation, innovation, and sustainability.
The event, titled “New and Improved – AMCP Format for Formulary Submissions v5.0,” aims to educate pharmaceuticalmanufacturers and other healthcare stakeholders on the latest updates and best practices in dossier development. released in April 2024, marks the first update since 2020. The latest iteration, version 5.0,
Gaulkin — Enacted in 2022, the Inflation Reduction Act (IRA) amended the Medicare provisions of the Social Security Act to impose several discount requirements on pharmaceuticalmanufacturers. On July 31, 2024, CMS published a proposed rule to codify its guidances, with some changes.
Kirschenbaum — Last week, the United States Court of Appeals for the District of Columbia ruled that Section 340B of the Public Health Service Act does not prohibit pharmaceuticalmanufacturers from imposing conditions on the distribution of discounted drugs to covered entities in the program. In United Therapeutics Corporation v.
Gaulkin — On April 10, the Fourth Circuit unanimously affirmed a summary judgment ruling for the Centers for Medicare & Medicaid Services (CMS) regarding the agency’s definitions of “line-extension drug” and “new formulation” for purposes of determining rebates that drug manufacturers may owe the Medicaid Drug Rebate Program (MDRP).
Dr. Christina Beato: Lowering Interchangeable Biosimilar Standards Risks Patient Health, Physician Confidence On January 17th, the Albuquerque Journal published an op-ed by Dr. Christina Beato, former Assistant Secretary for Health and Human Services (HHS) on the topic of interchangeable biosimilar standards.
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