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Power to the Patient with Patient Generated Health Data

FDA Law Blog: Biosimilars

Lenz, Principal Medical Device Regulation Expert — FDA’s Center for Devices and Radiological Health (CDRH) recently partnered with the Digital Medicine Society (DiMe) to host a two-day workshop to help advance the use of patient-generated health data (PGHD) to support improved clinical trials, medical device development, and regulatory science.

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Shaping the Future: Eli Lilly's Role in the Weight Management Revolution

DrugBank

The weight loss industry has emerged as a major hub for innovative research, groundbreaking treatments, and economic opportunity. billion in 2022 and is projected to grow at a compound annual growth rate of 9.94% from 2023 to 2030. With sales soaring to $2.2 for this class of drugs.

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The Race for Ozempic Alternatives: Unlocking the Future of Weight Loss Medication

DrugBank

adults using obesity medications by 2030, further underlining the growing significance of this sector. Inspired by its success, pharmaceutical companies are pursuing the development of drugs with similar therapeutic profiles, aiming to expand treatment options. Goldman Sachs analysts anticipate a significant rise in the number of U.S.

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Roche awarded WHO prequalification for the HIV and HCV tests on the cobas 6800/8800 Systems

The Pharma Data

WHO prequalification helps regulators and procurers in low and middle-income countries to identify products that meet high quality standards and are safe and suitable for their intended use. Roche’s Global Access Program provides innovative diagnostic solutions improving disease and patient ma. management for those most in need.

Disease 52
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Learning from history: Sanitation for prosperity

The Pharma Data

The disposal and treatment of human waste has been an integral part of human civilization for thousands of years. With only 10 years left until 2030, the rate at which access to sanitation is increasing will need to quadruple if the world is to achieve the Sustainable Development Goal (SDG) sanitation target. Source link.

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Distinguishing the Roles of Preclinical vs. Clinical CROs in Clinical Research

Vial

In the field of clinical research , this pipeline can be broken down into several stages and processes specifically designed to rigorously validate the safety and efficacy of new drugs and treatments. billion by 2030 at a compound annual growth rate (CAGR) of 7.5% between 2024 and 2030. What is a Pre-Clinical CRO?

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Article Periodic Thank You Why comprehensive state-level bans on PFAS in products are faltering

Agency IQ

Generally, how have states attempted to regulate PFAS? States are attempting to regulate PFAS in a variety of ways, including via multiple in-state regulatory and legislative avenues. In addition, the law prohibits the sale of carpets or fabric treatments containing PFAS as of January 1, 2023.