Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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If you'll be at DIA in June, I hope you'll join CluePoints and Advarra for an evening of excitement, celebration, and valuable networking with our peers in the healthcare industry, regulatory government, academics, patients, and more! Get the info and sign up: https://cvent.me/AN7Be1#clinicalresearch #clinicaltrials #dia2024
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Pediatric Cell and Gene Clinical Research: trial execution, regulatory requirements, challenges, risks, and benefits us02web.zoom.usGet the latest on pediatric cell and gene clinical research in this webinar hosted by Institute for Advanced Clinical Trials for Children (I-ACT for Children) on June 25! Advarra's Executive Director of Biosafety Services Dr. Daniel Eisenman will share his biosafety insights with the panel #pediatrictrials #educationalwebinar #CGT
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Reporting to the IRB: Investigator Noncompliance https://www.advarra.comNeed a refresher on IRB noncompliance reporting? Check out our recently revised blog:
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Collection of Race and Ethnicity Data in Clinical Trials and Clinical Studies for FDA-Regulated Medical Products January 2024 fda.govRace & ethnicity impact how individuals respond to medical products. FDA's new draft guidance recommends standardized data collection and reporting to ensure equitable healthcare outcomes. Your input matters!
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Striking the Balance: Ethics, Inclusion, and Vulnerability in Research info.advarra.comHow do we as a research community balance the need for greater inclusivity with protecting vulnerable participants? Join our 4/11 webinar for a fascinating discussion by Luke Gelinas:
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Understanding FDA’s 2024 Draft Guidance on DMCsUntil 2024, FDA hadn't updated its DMC guidance in almost 20 years. Find out what the agency changed (and what it didn't) in our blog #DMC #clinicaltrials #regulatory
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Enhancing Research Ethics: Understanding HRPP Staffing and the sIRB Mandate https://www.advarra.comJust because an sIRB is reviewing the study doesn’t mean the local IRB has nothing to do. Read our blog for more on HRPP roles:
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Striking the Balance: Ethics, Inclusion, and Vulnerability in Research info.advarra.comHow do we as a research community balance the need for greater inclusivity with protecting vulnerable participants? Join our 4/2 webinar for a fascinating discussion by Luke Gelinas:
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Comprehensive Global Review Services https://www.advarra.comAdvarra is more than an IRB – we’re your one-stop shop for DMC, EAC, CEC, and IBC. Other providers can’t match our expert network and integrated solutions.
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Lauri Carlile
Executive VP @ Advarra | IRB, IBC, DMC, EAC
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Faster Trials, Successful Sites, Empowered Patients: Improve Your Research Experience info.advarra.comI know organizations like yours are looking for ways to speed up trials while keeping sites on track. At Advarra, we believe better site performance and compliance start with you – the study team. Don’t miss our upcoming webinar on February 22, where we will review industry trends and real study use cases on how to improve operational outcomes by focusing on the research experience.
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