June 1: Avoiding Common Mistakes in Clinical Research: An FDA Perspective Webinar, 12 p.m.-1:30 p.m.

Contact: ACRP 1-2: 2nd DIA Cardiac Safety Workshop in Japan, Tokyo, Japan. Contact: DIA 1-2: FDA Inspections of Clinical Data Systems, Dublin, Ireland. Contact: CfPIE 2-3: Practical Methods for Project Management, King of Prussia, PA. Contact: CfPIE 3-7: 2011 American Society of Clinical Oncology Annual Meeting, Chicago, IL. Contact: ASCO 6-7: DIA European Regulatory Affairs Forum 2011, London, UK. Contact: UK 6-8: Drug Development Decisions: The NDA Simulation Workshop, Arlington, VA. Contact: PERI 6 -8: Good Clinical Practices (GCP), Los Angeles, CA. Contact: CfPIE 6-9: 2011 ISPE Washington Conference, Washington, DC. Contact: ISPE 8: Effective EDC Training Strategies Webinar, 12:00 p.m.-1:30 p.m. Contact: ACDM 8: Learning to Communicate Effectively in Multidisciplinary Teams Webinar, 12 p.m.-1:30 p.m. Contact: ACRP 8: Complimentary Webinar: Patient Recruitment and Rapid Study Start Up for Specialized Products, 12 p.m.1 p.m. Contact: CBI 8: Complimentary Webinar: Patient Reported Outcome Assessments in Clinical Trials, Navigating the EMA and

FDA Regulatory Framework, 10 a.m.-11 a.m. Contact: CBI 8-10: EudraVigilance TrainingElectronic Reporting of ICSRs in the EEA, London, UK. Contact: DIA 9-10: Pharmokinetics in Drug Developmentan Integrated Approach, London, UK. Contact: BIO 9-10: Standard Operating Procedures (SOPs) Development and Implementation, Halifax, Canada. Contact: SoCRA 9-10: Adverse Drug EventsUnderstanding and Reporting Requirements,Los Angeles, CA. Contact: CfPIE 13-14: Pediatric Pharmaceutical Development, Arlington, VA. Contact: PERI 13-14: 8th Patient Reported Outcomes, Philadelphia, PA. Contact: CBI 13-14: Mastering Clinical Trial Monitoring, Boston, MA. Contact: CHI 15: Global Recruitment and Retention: Indispensible Strategies for Reducing Clinial Trial Timelines Webinar, 12 p.m.-1:30 p.m. Contact: ACRP 15-16: Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard CertificationsKing of , Prussia, PA. Contact: CfPIE 15-16: Diabetes Clinical Experience Program, Derby, UK. Contact: BIO 15-17: IVTs 2nd Annual ACE: Aseptic Processing, Cleaning Validation, Environmental Monitoring and Microbiology Compliance,Philadelphia, PA. Contact: IVT 16: Training Course for eCTD Submissions in

Switzerland, Bern, Switzerland. Contact: DIA 16-17: Advanced Site Management: Finance and Productivity Enhanced Business Practices for Clinical Research Programs,Chicago, IL. Contact: SoCRA 16-17: Clinical Research Monitoring and GCP Workshop for Monitors,Site Coordinators and Auditors , New Orleans, LA. Contact: SoCRA 17-19: Fundamentals of Clinical Research Monitoring, Chicago, IL. Contact: DIA 17-19: Introduction to Good Clinical Practices and Auditing, Chicago, IL. Contact: DIA 17-19: Regulatory Affairs Part I: The IND Phase, Chicago, IL. Contact: DIA 17-19: Clinical Project Management, Chicago, IL. Contact: DIA 18-19: Risk Management and Safety Communication Strategies, Chicago, IL. Contact: DIA 18-19: New Drug Product Development and Lifecycle Management, Chicago, IL. Contact: DIA 19: Act of Writing a Clinical Overview, Chicago, IL. Contact: DIA 19-23: 47th DIA Annual Meeting, Chicago, IL. Contact: DIA 20-21: Oncologic Development Strategies: Protocol Development, Arlington, VA. Contact: PERI 20-21: Preparation of FDA Submissions and Communicating with the FDA (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements, Los Angeles, CA. ) Contact: CfPIE 20-22: EudraVigilance TrainingElectronic Reporting of ICSRs in the EEA, London, UK. Contact: DIA

20-22: Good Laboratory Practices, New Brunswick, NJ. Contact: CfPA 21-23: Preparation, Packaging, and Labeling of Clinical Trial Materials, New Brunswick, NJ. Contact: CfPA 21-22: Project Management for Phase I and II Clinical Trials, Los Angeles, CA. Contact: CfPIE 21-22: Level One Certificate in CDM-ing course 21-22: 2nd Annual Life Sciences Forum on Social Media Regulations and Compliance, Alexandria, VA. Contact: CBI Part 1 of 8, 12:00 p.m.-1:30 p.m. Contact: ACDM 21-23: Regulatory Strategy for Established Active Substances, Amsterdam, The Netherlands.Contact: TOPRA 22-23: Biomarker Applications on Drug Development, Arlington, VA. Contact: PERI 22-24: The Drug Development ProcessFrom Discovery to Commercialization,King of Prussia, PA. Contact: CfPIE 23-24: Project Management, San Diego, CA. Contact: ACRP 23-24: Fundamentals of Clinical Research, San Diego, CA. Contact: ACRP 23-24: Latin AmericaUnderstanding Regulatory Compliance Requirements,King of Prussia, PA. Contact: CfPIE 23-24: Auditing and Inspecting Preclinical Research for GLP Compliance, New Brunswick, NJ. Contact: CfPA 27-29: Packaging of Pharmaceuticals, New Brunswick, NJ. Contact: CfPA 28-29: Good Clinical Practices for Study Directors,

Principal Investigators, Study Staff, and Management, Cambridge, UK. Contact: BARQA 28-30: 2011 BIO Annual Convention, Washington, DC. Contact: BIO 30-July 1: Good Clinical Practice Regulatory Inspections, Cambridge, UK. Contact: BARQA July 1-2: Partnerships in Clinical Trials Latin America, So Paulo, Brazil. Contact: IIR 1-2: International Clinical Trials Workshop, Luj-Napoca, Romania. Contact: ASCO 1-2: Advanced Cancer Course International Clinical Trials Workshop (Romanian Society for Radiotherapy and Medical Oncology,Cluj-Napoca, Romania.Contact: ASCO 5-6: The Practical Application of Quality Risk Management Tools and Techniques, Cambridge, UK. Contact: BARQA 6-8: EudraVigilance TrainingElectronic Reporting of ICSRs in the EEA, London, UK. Contact: DIA 7: Safety Reporting in Clinical Trials, Heathrow Airport, UK. Contact: BARQA 7-8: Clinical Trials Japan 2011, Tokyo, Japan. Contact: BIO 9-10: Best of ASCO China,Hengzhou, China. Contact: ASCO 11-12: Asthma and COPD: Clinical Drug Development, Arlington, VA. Contact: PERI 11-15: Clinical Science Courses,Chicago, IL. Contact: SoCRA

13: Clinical Evidence to Support the Development of Medical Devices, Stansted Airport, UK. Contact: BARQA 18-19: Cancer 101:A Basic Overview of Current Therapies for New Oncology Researchers, Arlington, VA. Contact: PERI 18-19: Clinical Site Management Summit, Arlington, VA> Contact: CBI 18-20: WORLDx Congress, Baltimore, MD. Contact: IIR 21-22: SoCRA Clinical Site Coordinator/Manager Program for Coordinators,Research Associates, Study Nurses, and Site Managers Registration Toronto, , Ontario. Contact: SoCRA 25-27: ePharma Summit West, Santa Clara, CA. Contact: IIR 29-30: 2011 Best of ASCO Miami, Miami, FL. Contact: ASCO