spacer
home > news > detailed info
INDUSTRY NEWS AND PRESS RELEASES

Signant Health Appoints Todd Everhart as Clinical Vice President to Accelerate Intelligent eCOA and Predictive Data Analytics in Medical Clinical Research

Signant Health

Award-winning Science and Medicine Team expands its expertise


PHILADELPHIA, PA – August 20, 2019: Signant Health, formerly CRF Health and Bracket, has appointed Anthony Todd Everhart, MD, FACP to the Signant Health Science and Medicine Team as Clinical Vice President, Internal Medicine, reporting to the Chief Medical Officer, Dr. David Daniel.

As a technology company, Signant is unique in its commitment to data quality, consistency and integrity due to its internal team of renowned scientists, experienced clinicians and analytics experts. Signant provides customers with an extra layer of confidence through proactive and near real-time monitoring and assessments of incoming clinical data. With its eCOA and Endpoint Quality solutions, Signant identifies risks and provides actionable remediation recommendations where appropriate to avoid and correct potential issues before they become threats that can negatively impact the trial.

Dr. Everhart is Board-certified in Internal Medicine and a Fellow of the American College of Physicians with over 23 years of experience in the practice of medicine and over 12 years of experience in clinical development. Prior to joining Signant, Dr. Everhart held positions of Vice President, Medical Affairs and Vice President, Medical Informatics at Chiltern and Covance, and most recently consulted independently in the areas of Medical Monitoring, Medical Data Review, and Physician Adoption of Technology. He has worked in all phases of clinical development in numerous therapeutic areas including Allergy & Immunology, Cardiovascular, Hematology & Oncology, Infectious Disease & HIV, Neurology, Ophthalmology, Psychiatry, Respiratory, and Rheumatology. With Signant Health, Dr. Everhart will help accelerate the application of Signant’s intelligent eCOA, rater training, predictive analytics and other data quality monitoring products outside of CNS disorders.

Speaking on this appointment, Mike Nolte, CEO of Signant Health, said, “Biopharmaceutical sponsors’ focus on complex indications continues to accelerate challenges with speed, quality and risk, as they work designing studies that result in breakthrough therapies. Signant recognizes that deep expertise and innovative technology can combine to ensure constant monitoring, real-time feedback and oversight that promote confidence and quality in this increasingly complex environment. We believe that bringing outstanding technical and clinical minds together creates expertise to design and deploy proven methodologies, while innovating in differentiated technologies like intelligent eCOA, evaluating data quality and consistency as it is generated. Dr. Everhart, as one of those outstanding, proven experts will be a great asset to Signant’s award-winning clinical teams and to our work to leading the market in predictive, intelligent analytics.”

Dr. Daniel adds, “Medical clinical trials, like CNS trials, require modulation of placebo response and precision in examination and measurement skills in order to succeed. Dr. Everhart will apply to internal medicine clinical trials many of the rater calibration, data analytic and intelligent eCOA techniques that have positively impacted CNS trials. Dr. Everhart will promote a collaborative, risk-based approach to improve data quality.”

Dr. Everhart concludes, "I am proud to bring my expertise to Signant’s established Science and Medicine Team, working alongside innovators in their fields. Signant’s ground-breaking solutions provide unique advancements in eClinRO services and the collection of precise, reliable assessments across multi-site and global development programs. The challenge to me is to expand our portfolio of rater training, data quality monitoring, and data quality analytics across a wide range of therapeutic areas beyond Neurology and Psychiatry which will allow new medicines and therapies to be introduced to the market with more confidence and quality. I am excited to rise to this challenge within such an experienced team.”

Signant is a global technology company that accelerates clinical research and improves the experience of patients accessing potentially life-changing therapies. Its solutions, combined with deep scientific and clinical insight, link engaged patients to researchers, provide faster, more reliable decision making, and help provide longer, healthier and more productive lives for families and communities around the globe.

To learn more about Signant Health and the most comprehensive patient-technology suite for eCOA, eConsent, Patient Engagement, IRT, Clinical Supply Management, and Endpoint Quality solutions, visit www.signanthealth.com.

*****************

Who Is Signant Health?

The best technology succeeds in the background. Signant Health (formerly CRF Health and Bracket) provides solutions that simplify every step of the patient journey to make it easier for people to participate in, and for sites and study teams to run, clinical trials. Signant unites eCOA, eConsent, Patient Engagement, IRT, Clinical Supplies and Endpoint Quality into the industry’s most comprehensive patient-centric suite – an evolution built on more than 20 years of proven clinical research technology. Our intense focus on the patient experience, deep therapeutic area expertise and global operational scale enable hundreds of sponsors and CROs (including all Top 20 pharma) to extend the reach of drug development, expand patient opportunities and improve data quality – helping them bring life-changing therapies to our families and communities around the world. Take a significant step toward patient-centricity at signanthealth.com.

CRF Health and Bracket are now Signant Health.

Contact: media@signanthealth.com, +1 267.498.2350

phone +1 267 498 2300
email media@signanthealth.com
web https://signanthealth.com/
email 4000 Chemical Road Suite 300 Plymouth Meeting, PA 19462
 
Print this page
Send to a friend
   
spacer
News and Press Releases

Nova Biomedical Launches BioProfile® FLEX2 On-Line Autosampler for Fully Automated Sampling, Analysis, and Feedback Control of up to 10 Bioreactors

Waltham, MA Nova Biomedical is pleased to announce the launch of the BioProfile FLEX2 On-Line Autosampler (OLS), a modular system that connects as many as 10 bioreactors to one FLEX2 analyzer for up to 3 weeks of walkaway, automated sampling, analysis, and feedback control of key cell culture analytes. The FLEX2 measures up to 16 tests including pH, gases, metabolites, osmolality, cell density, and cell viability.
More info >>


White Papers

Running Better Trials Taking an Intelligent Monitoring Approach

Bioclinica

When it comes to implementing a risk-based monitoring program, it is not just about reducing monitoring visits and doing less Source Document Verification (SDV). It’s about bringing together your people, a solid process, and the right technology to run a better trial. Success with risk-based monitoring requires the ability to make sense of the thousands, if not millions, of data points captured by multiple disparate sources in a clinical trial. With the sheer volume of data generated on a daily basis comes complexity. How does one make sense of it all? Information overload burdens even the most experienced study teams who struggle to understand which data matters most and what it means.
More info >>

Industry Events

Outsourcing in Clinical Trials West Coast

3-4 March 2020, Hyatt Regency San Francisco Airport

Last year's event was attended by 700+ clinical trial stakeholders. Following its success, we are pleased to forecast the 2020 edition will be even in larger scale, with a great speaker line up and engaging content. This edition aims to give attendees practical take-aways which they can apply to their studies.
More info >>

 
©2000-2011 Samedan Ltd.
Add to favourites

Print this page

Send to a friend
Privacy statement