A US-based biotech looked for a trusted regulatory partner to:
1) Build and execute an EU regulatory strategy and roadmap in view of obtaining new drug approval in Europe.
2) Manage related clinical trial application and clinical safety activities at a global level.
Resources
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The European Union is transforming its health technology assessment process with the introduction of the Joint Clinical Assessment (JCA) under…
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In the fast-paced world of biotech innovation, time is of the essence. For European biotech ventures eyeing entry into the…
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Embarking on the journey to expand into the United States market is a pivotal moment for any European biotech company.…
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Phages, also known as Bacteriophages, are viruses that infect specific bacteria and provoke their death via lytic activity. They are…
