EOM 1352: Fri 7 June 2024, 11:36

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Challenges in the Post-marketing Investigations for Medical Devices

As the European and overall worldwide regulation strives to become clearer, unambiguous, harmonised and as a result, more restrictive and demanding, this tendency st...
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The Clinical Development Market in APAC: Opportunities, Growth and Challenges

The Asia-Pacific (APAC) region has rapidly emerged as one of the most dynamic markets in global clinical development. Over the past decade, demand for innovative the...
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Regulatory Perspectives on the FDA’s Use of Artificial Intelligence in Drug Development

As artificial intelligence (AI) gains prominence in drug development, regulatory agencies such as the US Food and Drug Administration (FDA) are creating and implemen...
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The Importance of Clinical Trial Preparation for Biotech Companies – A UK Perspective

The UK biotech sector is thriving and with significant investment flowing into research, the opportunities for growth and innovation are considerable. In 2024, UK bi...
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A CRO Should be the Partner that Gives Full Visibility on a Gene Therapy Trials Path

 Ahead of ARVO 2025 next week where Emmes is poised to launch the first dedicated ophthalmology clinical trial technology platform, we spoke with Saqib Parkar, ...
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Accelerating Safely Toward an Efficient Ethical Review Framework

“All organisations, even the most renowned and successful, sometimes make the right things too hard and the wrong things too easy.”1 Sutton and Rao address this prob...
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