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What to expect in 2018

Across the two days, senior-level representatives and decision makers in Minnesota area will come together to discuss some of the most pressing challenges, objections and practical steps the sector can take towards product development.

Day one will focus on industry trends and global regulatory changes. You will find sessions highlighting new requirements of the MDR and new guidance of FDA. We will compare both markets to investigate which one will be faster to launch your product and what to prepare for it. In the afternoon, we will explore new technologies in clinical trials and data management systems which will be the key to conduct cost-effective trials.   

Throughout the second day, we will focus on outsourcing and study management strategies through changing environment. We will analyse the best mix of internal & external staff for your study and what would be the criteria to get partners on board. Along with that, you will see best practices on using CROs in pre-clinical and post market activities to get better invest return.

Countdown to Outsourcing in Clinical Trials Medical Devices USA 2018

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