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DIA 2012 is the largest multidisciplinary event for professionals involved in the discovery, development, and life cycle management of pharmaceuticals, biotechnology, medical devices, and related products. This year’s event will help you develop a holistic and integrated program for your entire team while increasing everyone's access to training and expanded professional opportunities.

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Title Event Type Day Time Track(s) Credits
#20: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development Tutorial Sunday, Jun 24 8:30AM - 12:00PM Track 08 - Regulatory Affairs and Submissions IACET
#21: FDA Enforcement: Understanding the Agency's Authority, How Violations Occur, How to Prevent Them, and How to Respond If Violations Do Occur Tutorial Sunday, Jun 24 8:30AM - 12:00PM Track 08 - Regulatory Affairs and Submissions IACET
#22: Utilizing Chemistry, Manufacturing, and Controls in Drug Development Tutorial Sunday, Jun 24 8:30AM - 12:00PM Track 12 - Pharmaceutical Quality IACET
#23: Global Market Access: Essential Knowledge for Clinical Trial Design Tutorial Sunday, Jun 24 8:30AM - 12:00PM Track 13 - Health Economics and Outcomes (HEO)/Comparative Effectiveness Research (CER)/Health Technology Assessment (HTA) IACET
#24: A Device Primer: 510(k)s, PMAs, IDEs Tutorial Sunday, Jun 24 8:30AM - 12:00PM Track 09 - Medical Diagnostics and Devices CME, IACET
#40: Understanding and Navigating the Regulatory System in China Tutorial Sunday, Jun 24 9:00AM - 5:00PM Track 08 - Regulatory Affairs and Submissions IACET
#41: Quality Oversight of CROs - Clinical Vendors Tutorial Sunday, Jun 24 9:00AM - 5:00PM Track 03 - Innovative Partnering Models and Outsourcing Strategies IACET
#42: Regulatory Affairs for Biologics Tutorial Sunday, Jun 24 9:00AM - 5:00PM Track 08 - Regulatory Affairs and Submissions ACPE, IACET
#43: Clinical Statistics for Nonstatisticians Tutorial Sunday, Jun 24 9:00AM - 5:00PM Track 01 - Clinical Operations ACPE, CME, IACET
#30: Regulatory Affairs in the European Union: An Overview of Registration Procedures for Medicinal Products in the EU Tutorial Sunday, Jun 24 1:00PM - 4:30PM Track 08 - Regulatory Affairs and Submissions IACET
#31: Leadership: How to Organize and Lead People in Group Work Tutorial Sunday, Jun 24 1:00PM - 4:30PM Track 16 - Professional Development IACET, PMI
#32: Designing, Operating and Evaluating Patient Registries Tutorial Sunday, Jun 24 1:00PM - 4:30PM Track 13 - Health Economics and Outcomes (HEO)/Comparative Effectiveness Research (CER)/Health Technology Assessment (HTA) ACPE, CME, IACET, RN
#33: Understanding Comparative Effectiveness Research (CER) in the Biopharmaceutical Industry Tutorial Sunday, Jun 24 1:00PM - 4:30PM Track 13 - Health Economics and Outcomes (HEO)/Comparative Effectiveness Research (CER)/Health Technology Assessment (HTA) ACPE, CME, IACET, RN
#34: Fourteen Steps from Research to Development Tutorial Sunday, Jun 24 1:00PM - 4:30PM Track 08 - Regulatory Affairs and Submissions CME, IACET
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