ICR’s Ethics & GCP Forum Adapting to Structural and Regulatory Changes 13  February 2012 London Speaker: Nicky Dodsworth Topic: Key GCP Updates Click here for more information

ICR Symposium Quality Frameworks & Systems Thinking 28 February 2012 London, United Kingdom Speaker: Nicky Dodsworth Topic: Quality Frameworks & Systems Thinking Click here for more information

Partnerships in Clinical Trials Conference 4-7 March 2012 Orlando, FL Booth 707 Click here for more information

6th Annual Medical Device Clinical Research Conference 5-6 March 2012 Baltimore, MD Click here for more information

24th Annual DIA EuroMeeting 26–28 March 2012 Copenhagen, Denmark Speaker: Sherri Hubby Topic: A Global Perspective from Ethics, Accreditation Bodies and Industry on Conducting Clinical Trials to Ensure Compliance Poster: A Comparative Study of Ethics, Regulatory and Sponsor Considerations in Conducting Clinical Trials in Developing Countries Poster:A Comparison of Regulatory Evidence Techniques used by Pharma and Regulators Regarding Investigator Misconduct in Clinical Trials Click here for more information

ARC's 1st Annual East Coast Summit for Clinical Development Executives and Academic Medical Centers 3–4 April 2012 Philadelphia, PA Speakers: Dr. Charlene Sanders/Angi Robinson Topic: Successful Pediatric Studies: Key Study Design and Site Selection Considerations Speaker: Dr. Krista Armstrong Topic: Optimizing Patient Recruitment in the Traditional Markets Speaker: Dr. Jacqueline Zarro Topic: Managing High Performance Teams with a Focus on Maximizing Teams both Local and Global Click here for more information

ACRP 2012 Global Conference & Exhibition 14-17 April 2012 Houston, TX Speakers: Elizabeth Jay, RN, MA and Angi Robinson Topic: Successful Pediatric Studies: Key Study Design and Site Selection Considerations Click here for more information

SoCRA's Protecting Human Research Participants: Legal, Ethical and Practical Considerations SoCRA's Protecting Human Research Participants: Legal, Ethical and Practical Considerations 26-27 April 2012 Boston, MA Speaker: Ron Kershner, PhD Topic: The Role of the Data Monitoring Committee Click here for more information

31st Annual APS Meeting 16–19 May 2012 Honolulu, HI Booth 507 Click here for more information

SoCRA Regulations and Guidelines for Device Clinical Research 16-18 May 2012 Lake Buena Vista, FL Speaker: Angela Cho Topic: Special Considerations for Device Monitoring Speaker: Sarah Zanon Topic: Reporting Device-related Effects Click here for more information

MAGI's Clinical Research Conference - 2012 East 20–23 May 2012 Washington, D.C. Speaker: Dr. Krista Armstrong Topic: Productive Sponsor-Site-CRO Relationships Click here for more information

48th Annual DIA Meeting 24–28 June 2012 Philadelphia, PA Speaker: Jaclyn Brown Topic: Understanding the Challenges of Conducting Studies for Orphan Indications and Rare Diseases Speaker: Sunita Ahir, Ph.D. Topic: Two Arm Double Randomised Clinical Trial using Drugs and Devices Speaker: Sunita Ahir, Ph.D. Topic: A Review of the Recast of European Medical Device Directives Speaker: Jessica Merryfield Topic: Managing Biometric Timelines – Key Factors to Success Speaker: Sherri Hubby Topic: Conducting Clinical Trials in Developing Countries - A Comparison between the Expectations of the FDA, EMA and ANMAT Regulations Booth 1907 Click here for more information

14th World Congress on Pain 27-31 August 2012 Milan, Italy Booth 673 Click here for more information

SoCRA 21st Annual Conference 21–23 September 2012 Las Vegas, NV Speaker: Angela Cho Topic: Special Considerations for Device Monitoring Click here for more information