How Will the EU Biotech Act Transform Biotechnology Regulation in Europe?

How Will the EU Biotech Act Transform Biotechnology Regulation in Europe?

In this episode of Conversations in Drug Development, host Harriet Edwards is joined by Kelsey Lennoch and Eamon McGowran to discuss the EU Biotech Act, a major regulatory proposal aimed at revitalizing Europe’s biotech sector. They explore the act’s goals to streamline clinical trial processes, harmonize regulations, and boost funding for late-stage biotech companies. The conversation highlights key changes for medicines and medical devices, the act’s potential impact on innovation and competitiveness, and the importance of ongoing engagement as the EU’s regulatory landscape evolves. For more information, visit www.boydconsultants.com.

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Avsnitt(25)

UK Clinical Trial Regulation: What Sponsors Need to Know About UK CTR 2025

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Navigating the FDA Landscape: More Changes, and What's Next?

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At the forefront of innovation: Prof Alan Boyd reflects on the last 20 years in drug development

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Navigating the New FDA Landscape: Opportunities and Challenges Ahead

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From Lab to Launch – Avoiding the Pitfalls of Drug Development

From Lab to Launch – Avoiding the Pitfalls of Drug Development

In this episode, Dr Neil Fish and Dr Ami Patel dive into the real-world challenges of drug development - from early-stage planning to regulatory hurdles and everything in between. Drawing on decades o...

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Crystal Ball Gazing: What Does the Future Hold for Regulatory Affairs in Drug Development for 2025

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In this episode, Harriet Edwards from Boyds hosts a discussion on 2025 predictions in drug development and regulatory affairs. Joined by regulatory experts Dr. Katherine Bowen and Dr. Eric Hartder, th...

17 Mars 202532min

How to Effectively De-Risk your IND Process

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