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Improving the efficiency of the approval process for new medicines within the European Medicines Agency (EMA) involves several strategies...

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EMA's Clinical Trial Regulations (EUCTR) in European Union

The new EU Clinical Trial Regulation (CTR) 536/2014, which came into effect on January 31, 2022, represents a significant overhaul of the...

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Microbiome Based Therapies : Regulations and Market Outlook

Microbiome-based therapies are a promising area in precision medicine, aiming to tailor treatments based on individual microbial...

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Pharmaceutical Regulations and Registration in South Korea (MFDS)

The pharmaceutical market in South Korea was estimated to be worth 25.4 trillion South Korean won in 2021. The market size has been...

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