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Planning Gene Therapy Research? Prepare for institutional biosafety committee (IBC) Review with these tips from the Biosafety Officer at a leading IRB.
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Talking the Patients' Language – the importance of effective, patient-centered engagement
Live Webinar: Tuesday, June 6 at 8:00 am EDT
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Winning the RAT race: A new Center of Excellence to drive development of regenerative medicines
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Medical Devices |
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New Trials Law in France: Advantages for Medical Device Studies |
The new law on research in France introduces changes for the medical device industry by facilitating the conduct of postmarketing studies. Devices will no longer have to be provided free of charge for low-risk interventional studies making France a possible location for such trials in the future.
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Is Your CTMS Working for You? Unify and Optimize Your Approach to Clinical Trials
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