News & Updates

FDA requires more postmarket data to keep certain devices on the market

09/16/2019

Medical Design & Outsourcing has published an article regarding FDA’s recent announcement require Medical Device manufacturers to provide more Real World Evidence for certain premarket approvals or risk losing those approvals. To read the entire article, click the button below. Continue Reading The Entire Article

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Meet with Christopher Kata, at SCDM 2019 on September 29th to October 2nd in Baltimore, MA!

09/09/2019

Meet with Christopher Kata, Director of Sales & Marketing on September 29th to October 2nd, 2019 in Baltimore, MA! Christopher Kata, Director of Sales & Marketing905 [email protected] SCDM 2019When: September 28th to October 2nd 2019Where: Baltimore, MA Christopher Kata is in Baltimore for SCDM 2019 both days and currently has several openings in his schedule.…

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AI in Drug Discovery and Development: Emerging Technologies and Applications

09/03/2019

This year at DIA one of the overriding themes was with the value and benefit of Machine Learning and Artificial Intelligence. One of these sessions was of particular interest and a summary has since been published by DIA. “Assembling experts from the application and research side of drug discovery, the session AI in Drug Discovery…

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Good Example of Integrating Wearable Devices (cameras) with Machine Learning Into Patient Care – The Potential For Use In Clinical Trials

08/31/2019

In a News Release on Eureka Alert, comes a fascinating example of how cameras were used in patient care combined with machine learning to better identify and improve lifestyle strategies for heart failure patients. The article titled “Tiny wearable cameras may improve quality of life in heart failure patients” and is an outstanding example of…

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Meet with Christopher Kata, August 27th to 28th, 2019 in Philadelphia, PA!

08/18/2019

Meet with Christopher Kata, Director of Sales & Marketing on August 27th – 28th, 2019 in Philadelphia, PA! Christopher Kata, Director of Sales & Marketing905 [email protected] When: August 27th to 28th 2019Where: Philadelphia, PA Christopher Kata is in Philadelphia for meetings both days and is available for additional meetings. If you’re interested in having a…

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Meet with Christopher Kata in Tampa, Florida August 19th – 21st.

08/18/2019

Meet with Christopher Kata, Director of Sales & Marketing on August 19th – 21st, 2019 in Tampa, Florida! Christopher Kata, Director of Sales & Marketing905 [email protected] When: August 19th to 21st 2019Where: Tampa, Florida Christopher Kata is in Tampa for meetings all three days and has some availability for additional meetings. If you’re interested in…

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What Is Taking So Long For Meaningful Interoperability In Clinical Research?

08/16/2019

From Clinical Leader comes a very timely article on the state of interoperability within clinical research Clinical Trials today can benefit tremendously as a result of the value produced from integration with EMR systems, leveraging Real World Data and Real World Evidence, and the adoption of eSource! “Three decades ago when I entered the profession…

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Meet with Christopher Kata at “DIA 2019” in Booth # 2633 on June 23rd – 27th in San Diego, CA

06/19/2019

Meet with Christopher Kata, Director of Sales & Marketing on June 23rd – 27th 2019 at “DIA 2019” Booth # 2633 in San Deigo CA! Christopher Kata, Director of Sales & Marketing 905 999-1957 [email protected] When: June 23rd – 27th 2019 Where: Booth # 2633 San Deigo Convention Center, 111 W Harbor Drive, San Deigo,…

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WideTrial Partners With Oncotelic to Bring Expanded Access Platform to Cancer

06/14/2019

WideTrial , one of TrialStat’s strategic partners has partnered with Oncotelic to bring the Expanded Access Platform to Cancer. June 03, 2019 (ACCESSWIRE via COMTEX) — SAN FRANCISCO, CA / ACCESSWIRE / June 3, 2019 / WideTrial Inc., a third-party sponsor of Expanded Access programs, has begun a partnership with Oncotelic Inc., a wholly owned subsidiary…

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FDA to Launch Expanded Access Pilot ‘Project Facilitate’

06/02/2019

The goal of Project Facilitate is to make it easier for oncologists or healthcare providers without the regulatory experience or resources to navigate the single patient IND process. “Access to clinical trials and access to novel therapeutics for patients is still a problem. We know that not all oncologists or healthcare providers have the regulatory…

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