(IN BRIEF) EMA, together with the European Commission and the Heads of Medicines Agencies, has released the first report measuring progress toward the EU’s 2030 clinical trial targets. The report shows that 19 additional multinational clinical trials have been authorised … Read the full press release →
Posted in Business, European Union, Financial, Government, Healthcare, Industrial, Investment, Management, Marketing, Pharma & Biotech, Science, Technology, United Kingdom
Tagged Accelerating Clinical Trials in the EU, ACT EU, biotechnology, clinical research, clinical trial authorisation, clinical trial reform, clinical trial timelines, drug development, EMA, EMA and EU Authorities Advance Clinical Research Reforms Under 2030 Trial Strategy, EMA Highlights Early Progress in EU Efforts to Expand and Accelerate Clinical Trials, EU Biotech Act, EU clinical trials, EU Reports Early Progress Toward 2030 Clinical Trial Goals, European Commission, European Medicines Agency, European Union, FAST-EU, Heads of Medicines Agencies, Healthcare Innovation, healthcare policy, healthcare regulation, HMA, innovative medicines, life sciences, medical research, Medicine Development, multinational clinical trials, Patient Recruitment, pharmaceutical innovation, pharmaceutical sector, regulatory transparency, research investment
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