Pharmaceutical Science

Regulating and Authorizing Medicines: A Comparison of the FDA and EMA

March 13, 2023 - Medicine regulation, review, and authorization are critical tools for bringing drugs to market, monitoring patient safety, and ensuring the best health outcomes. While regulatory guidance can vary globally, comparing protocols can help assess the reliability of each pathway. The Food and Drug Administration (FDA) is responsible for evaluating and regulating medicines in the United...

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Verve Doses First Patient with Investigational Gene-Editing Medicine

by Veronica Salib

A recent statement by Verve Therapeutics announced the start of the phase 1b clinical trial on heterozygous familial hypercholesterolemia (HeFH) in New Zealand. This announcement highlighted the first...

Major Milestones in Medicine, Drug Development in Recorded History

by Alivia Kaylor

Because the past few centuries have witnessed several revolutionary scientific advances, research into the mechanisms responsible for infectious diseases and the development of drugs and vaccines has led to the eradication of...

Moderna Launches Foundation to Promote Access to Quality Care

by Samantha McGrail

Moderna recently launched the Moderna Charitable Foundation to promote public health, access to quality healthcare, and educational opportunities, particularly in underserved populations. The...

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