Greater scrutiny of financial ties to clinical investigators coupled with increased accountability and drug safety puts more pressure on contracting executives to clearly outline responsibilities from the start.
Attend Clinical Trial Cost & Contract Management and take back to the office the necessary tools to streamline processes and better define accountability and responsibilities.
* Gain the upper hand in your contract with a workshop dedicated to contract approach and development
* Avoid embarrassing and costly violations regarding financial ties to clinical investigators with a firm grasp on Fair Market Value (FMV)
* Bring your drug to market before your competitors by fine tuning you’re strategy for handling Intellectual Property (IP)
* Improve the quality of you’re 3rd party clinical research data with warning signals and outline methods direct from an FDA representative
* Improve ROI by defining best practices for handling site payment disputes with your CRO
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The Partnerships in Clinical Trials Blog focuses optimization intelligence, regulatory trends and globalization strategies for both as sponsors and CROs. It is an extension of the Partnerships in Clinical Trials Conference.
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Would you like to guest blog on our site? Or send us feedback? Send an email to jpereira@iirusa.com.



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