New Tufts Study: Assessing CRO Oversight Effectiveness and Impact, New Webinar Hosted by Xtalks

Experts from Comprehend and Tufts CSDD to discuss the recent study, outline where the industry is headed and ways to overcome oversight challenges including transparency, risk, and compliance

Xtalks Life Science Webinars

The live broadcast taking place on Thursday, March 29, 2018, at 1 p.m. EDT will present the results of a recent study conducted by the Tufts Center for the Study of Drug Development (Tufts CSDD) that benchmarks CRO oversight practices and their impact and effectiveness.

With increased attention on response to ICH E6 (R2) guidance and on achieving higher levels of transparency and speed, many pharmaceutical companies have begun to implement new CRO oversight practices and mechanisms.

Join Ken Getz, Director of Sponsored Research Programs & Associate Professor, Tufts CSDD as he discusses the results of the study and their implications. Specific areas covered include:

·         Types of CRO oversight models used for the variety of outsourcing approaches utilized

·         Oversight challenges including transparency risk and compliance areas

·         Industry experience with different oversight models and their reported impact and effectiveness

·         Performance metrics being gathered to measure oversight effectiveness

·         Insights into new approaches being implemented and planned to improve oversight effectiveness

For more information or to register for this complimentary event visit: New Tufts Study: Assessing CRO Oversight Effectiveness and Impact.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food, and medical device community. Every year thousands of industry practitioners (from life science, food, and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends, and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com

For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

Contact:

Nima Rajan

Tel: +1 (416) 977-6555 ext 352

Email: nrajan@xtalks.com

Source: Xtalks

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Categories: Pharmaceuticals and Biotech, Healthcare and Medical Informatics

Tags: clinical study, clinical trials, Comprehend, FDA guidance, ICH E6 (R2), Tufts CSDD, Xtalks


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Xtalks is a leading provider of educational webinars to the global life science, food and medical device community.