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SCOPE Summit for Clinical Trials Operations Executive

SCOPE Summit for Clinical Trials Operations Executive
February 23, 2016 - 1:00am (EST) to February 25, 2016 - 1:00am (EST)

Miami, FL

Booth #404

Bioclinica will introduce its latest offering, Post-Approval Research, at the 7th Annual SCOPE Summit. Nayan Nanavati, COO, Bioclinica Post-Approval Research, will give a presentation entitled, "It's Time to Rethink How Post-Approval Studies Are Done" on Wednesday, February 24 from 9:45-10:10 am.

On Tuesday, February 23 at 12:05, be sure to catch Ron Burns, Vice President, Product Management, eHealth Solutions in his session, "Integrating Mobile Application Generated Patient Data into your Risk-Based Monitoring Strategy." In this session Ron will talk about how innovative patient-centered mobile applications - from the newest biosensors to complete digital health records - are connecting patients with physicians and other health providers. Integrating this data into your clinical applications, such as the patient diary in your EDC system or as alerts in your Risk-based Monitoring application, now offers new horizons in patient safety and trial quality. Don't miss this opportunity to learn what's happening on this front.

Visit Booth #404 to learn more or to request a one-on-one meeting or demonstration.

SCOPE offers three stimulating days of in-depth discussions in 12 different conferences focused on issues related to each aspect of clinical trial planning and management: Data Integration, Feasibility, Site Selection and Management, Patient Engagement, Recruitment and Retention, Mobile Tech, Project Management, Forecasting, Quality (QbD) in Trial Conduct, Risk-Based Monitoring, Post-Marketing Studies, and Pharmacovigilance.

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Leader in Clinical Trial
Management Solutions

Bioclinica is organized into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging & Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Molecular Marker Laboratory. Our eHealth segment comprises eClinical Solutions, Randomization & Trial Supply Management, Safety & Regulatory Solutions, and Financial Lifecycle Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

Great advice from our Dir. Cardiovascular Imaging on quality imaging acquisitions & assessments in clin trials. https://t.co/OVH7pZ3SL0
bioclinica (42 minutes ago)
Almost here! #PCTrials Pre-arrange a meeting w @bioclinica Drop by & s/w David Kiger & Mike Lange. Mike will give a… https://t.co/8ymd2Q9KcJ
bioclinica (52 minutes ago)
Almost here! #PCTrials Pre-arrange a meeting w @bioclinica Drop by & s/w David Kiger & Mike Lange. Mike will giv… https://t.co/MpxTDV1T1L
bioclinica (54 minutes ago)
RT @bioclinica: Keeping to timelines in #clinicaltrials is key but can be hard to achieve. Join Bioclinica's Justin Hunt a webinar Nov. 2…
bioclinica (57 minutes ago)
RT @Xtalks: Removing Risk from #ClinicalTrial Management System (CTMS) Implementations @bioclinica https://t.co/EfuSVMSL13
bioclinica (7 hours ago)
Our Research Dev. Director Marieke Cajal in a poster presentation at #CNS Summit showed, "How to Scale up Recruitme… https://t.co/ySQpGIjvt9
bioclinica (7 hours ago)

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Congressman Meehan and Bioclinica CEO John Hubbard at recent visit to Bioclinica's Audubon offices