PRA attends a variety of industry conferences each year. Our own experts often speak at various forums, including conferences, symposia, and webinars, offering their insights into the industry. Events afford us the opportunity to connect with our colleagues in pharma and biotech industries, and share ideas with other thought leaders in the industry. To contact someone about an event, please click here.
Jan
Feb
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Biotech Clinical Outsourcing Partnerships 1-2 Feb 2012 Munich, Germany Speaker: Michael Kirchengast, Vice President, Scientific Affairs Topic: Key Considerations in the Design, Execution and Interpretation of Global Feasibility Studies
Outsourcing in Clinical Trials West Coast 15-16 Feb 2012 Burlingame, CA Speaker: Gretchen Goller, Director of Therapeutic Expertise Topic: Conducting a step-by-step analysis of vendor management to unlock the Value of a Strategic Partnership Booth #36
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13th Annual Phase I & IIa Clinical Trials 21-22 Feb 2012 The Lancaster, London Speaker: Gerhard Arold, Senior Director of Medical Affairs, Central & Eastern Europe Topic: Taking a Biologic From FIM Directly Into Patients Booth #17
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CBI's 8th Late Phase Research Summit 28-29 Feb 2012 Amsterdam, Netherlands Speaker: Agnes Rivaille Scientific Affairs Director, Late Phase Services Topic: Enhance Site Motivation to Improve Long-Term, Non-Interventional Study Data Collection and Analysis
Mar
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Partnerships in Clinical Trials 4-7 Mar 2012 Orlando, FL Speaker: Gretchen Goller, Director of Therapeutic Expertise Topic: CASE STUDY: Experimental Operations: Piloting Innovation without Fear Booth #219
BioPharma Asia Convention 2012 20-21 Mar 2012 Singapore Speaker: Kenneth Lee, Senior Director, Scientific Affairs (Asia), Therapeutic Expertise Topic: Emerging South-East Asia: Capitalizing on the heterogeneity of different markets to achieve clinical trial excellence Booth #D7
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Late Phase Drug Development World Americas 20-22 Mar 2012 Boston, MA Speaker: Kathleen (Kushner) Mandziuk | Senior Scientific Affairs Director PRA Late Phase Services Topic: Regulatory-mandated post-marketing studies Booth #12
Exploratory Clinical Development World 23-24 May 2012 London, United Kingdom Speaker: Willem Jan Drijfhout, Senior Vice President, Early Development Services Topic: Strategies for Accelerating Proof of Concept (Fast Track) Booth #TBD