| 2010 Testimony & Presentations |
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ACRO members actively participate in legislative and industry events that concern drug development. The testimonies and presentations below highlight our actions at these events.
| ACRO Comments on EU Clinical Trials Directive | | January 8, 2010 | | | The European Commission’s 09/10/2009 Public Consultation on the Assessment of the Functioning of the “Clinical Trials Directive” provides a welcome opportunity to assess the effectiveness of the Clinical Trials Directive (2001/20/EC) and to propose options with the goal of improving the functioning of the Directive while minimizing unintended negative consequences that may hinder the advancement of medical science. ACRO’s member companies have greatly invested in the clinical development infrastructure in the EU and are committed to assisting the Commission with the development of improvements that support the vital continuance of research in the region. With this in mind, we are pleased to submit comments on the above-referenced topic during the public consultation. | | Read more ... | | Download PDF |
2009 Testimony & Presentations 2008 Testimony & Presentations 2007 Testimony & Presentations 2006 Testimony & Presentations 2005 Testimony & Presentations 2004 Testimony & Presentations 2002 Testimony & Presentations 2001 Testimony & Presentations
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