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Clinical Trials Press Releases

Tufts Research: Strategies From Data Management Leaders to Speed Clinical Trials, New Webinar Hosted by Xtalks

Tufts Research: Strategies From Data Management Leaders to Speed Clinical Trials, New Webinar Hosted by Xtalks

Join this live webinar upcoming on Wednesday, Dec. 19, 2018, at 1 p.m. EST to learn how top pharmas and CROs plan to speed database build and data collection, as well as their top challenges and future priorities. Ken Getz,…

iPatientAxis Applies Near-Time Medical Record Retrieval to Convert Trial Intenders to Enrollees

​A recent study looking at digital patient recruitment for clinical trials found that social media in particular offers significant upside when it comes to usability for trial education and ultimately, enrollment. The study, “Content That Clicks: Effective Social Marketing for…

Automating the IRT Receipt Process for Temperature-Monitored Shipments, New Webinar Hosted by Xtalks

Automating the IRT Receipt Process for Temperature-Monitored Shipments, New Webinar Hosted by Xtalks

Poorly managed temperature excursions can be detrimental to the success of a clinical trial. In the supply chain, managing the process for temperature-sensitive products is extremely intricate and time-consuming. Featured speakers from Suvoda will cover, in case study format, Grünenthal’s…

Max Tokarsky, CEO of InvestAcure, to Present Keynote at the 13th Annual Conference on Dementia & Alzheimer's Disease in Abu Dhabi

Max Tokarsky, CEO of InvestAcure, to Present Keynote at the 13th Annual Conference on Dementia & Alzheimer's Disease in Abu Dhabi

InvestAcure, PBC announced today that founder and CEO Max Tokarsky will present a keynote address at the 13th Annual Conference on Dementia & Alzheimer’s Disease in Abu Dhabi on December 13th. With no available cure, Alzheimer’s is the seventh leading cause…

5 Signs You Need to Re-Evaluate Your Clinical Trial Management and Simple Steps to Improve Efficiency, New Webinar Hosted by Xtalks

5 Signs You Need to Re-Evaluate Your Clinical Trial Management and Simple Steps to Improve Efficiency, New Webinar Hosted by Xtalks

​As clinical trials grow in complexity, managing trial operations becomes increasingly more burdensome on resources and more susceptible to risk and decreased efficiency. Evaluating your organization’s current process for managing clinical trials is the first step in determining if it’s…

How to Develop a Global Clinical Study Budget Like a Pro, New Webinar Hosted by Xtalks

How to Develop a Global Clinical Study Budget Like a Pro, New Webinar Hosted by Xtalks

Clinical research is a notoriously cost-sensitive industry. The Tufts Center for the Study of Drug Development estimated the average cost of bringing a new drug to market to be over $2 billion – and with clinical trial costs on the…

Simplifying Clinical Data Flow From EDC to SDTM, New Webinar Hosted by Xtalks

Simplifying Clinical Data Flow From EDC to SDTM, New Webinar Hosted by Xtalks

In a live webinar taking place on Thursday November 29, 2018 at 1pm EST, industry experts will discuss the challenge of simplifying clinical data flow from EDC to SDTM and offer some solutions. Recent trends in clinical trials - including…

Clinical Trials in Inflammatory Diseases: From Organ-Targeted to Mechanism of Action-Targeted Therapies, New Webinar Hosted by Xtalks

Clinical Trials in Inflammatory Diseases: From Organ-Targeted to Mechanism of Action-Targeted Therapies, New Webinar Hosted by Xtalks

Join industry experts from Syneos Health, Dr. Anna La Noce, Executive Medical Director, General Medicine - Immunology & Inflammation, and Dr. Marcin Ernst, Vice President, General Medicine - Immunology & Inflammation, for a live webinar on Friday, Dec. 7, 2018,…

Reducing the eTMF Operational Burden Using Risk-Based Approaches, New Webinar Hosted by Xtalks

Reducing the eTMF Operational Burden Using Risk-Based Approaches, New Webinar Hosted by Xtalks

Life sciences organizations from emerging biotech to tier 1 pharma face a common challenge: the number of resources needed to maintain a high-quality, inspection-ready trial master file (TMF) rises with every additional clinical study they manage. For smaller organizations, already…

Delivering Patient-Centric Late Phase Research Using the Latest BYOD ePRO, New Webinar Hosted by Xtalks

Delivering Patient-Centric Late Phase Research Using the Latest BYOD ePRO, New Webinar Hosted by Xtalks

Clinical research is going through a period of rapid digitization, across all phases of drug development. With increasing focus on Phase IV and real-world evidence (RWE) comes the need to capture more data at a higher level of quality directly…

Recent Changes to Drug Approvals in China: Regulatory Consultation, IND Submission and Acceptance of Foreign Data in NDA, New Webinar Hosted by Xtalks

Recent Changes to Drug Approvals in China: Regulatory Consultation, IND Submission and Acceptance of Foreign Data in NDA, New Webinar Hosted by Xtalks

Join regulatory affairs expert Peiling Shih, Executive Director of Regulatory Strategic Development, APAC, at Clinipace for a live webinar on Monday, Dec. 3, 2018, at 12 p.m. EST (5 p.m. GMT). Historically, the review and approval of a Chinese investigational…

Heidi V. Pickett, Assistant Dean of the MIT Sloan Master of Finance Program, Joins InvestAcure, PBC Advisory Board

Heidi V. Pickett, Assistant Dean of the MIT Sloan Master of Finance Program, Joins InvestAcure, PBC Advisory Board

InvestAcure, PBC announced today that Heidi V. Pickett, Assistant Dean of the MIT Sloan Master of Finance program, has joined the InvestAcure PBC advisory board. InvestAcure is building a spare change investment platform to enable those impacted by Alzheimer’s to…

Personalized Oncology – Why Tissue Is the Issue When Characterizing Tumor Expression Profiles, New Webinar Hosted by Xtalks

Personalized Oncology – Why Tissue Is the Issue When Characterizing Tumor Expression Profiles, New Webinar Hosted by Xtalks

The future of cancer therapy relies on a personalized oncology approach by understanding individual variances and making therapy decisions accordingly. In the past 10 years, clinical researchers have primarily searched for drug targets using DNA sequencing to identify therapy-relevant mutations.…

Beyond Integration: A Unified IRT and eCOA Platform, New Webinar Hosted by Xtalks

Beyond Integration: A Unified IRT and eCOA Platform, New Webinar Hosted by Xtalks

Join Jaime Cook, Vice President of Technical Delivery at YPrime for a live session on Thursday, November 29, 2018 at 11am EST (4pm GMT), as he discusses the benefits of building eCOA and IRT in a unified platform. Discussion focuses…

Developing Psychedelics Into Medicine: Potential and Pitfalls, New Webinar Hosted by Xtalks

Developing Psychedelics Into Medicine: Potential and Pitfalls, New Webinar Hosted by Xtalks

Psychedelics, a class of powerful psychoactive substances that alter perception and cognition, have largely been relegated to illicit recreational substances after laws in the 1960s banned their use. This class of drugs includes LSD, psilocybin (magic mushrooms) and MDMA (commonly known…

Nurocor Partners With Intilaris to Accelerate Clinical Trials

Nurocor announced today that it has entered into a partnership with intilaris LifeSciences GmbH. Nurocor is the leading Clinical Metadata Repository provider with a mission to bring order to clinical data. intilaris LifeSciences is a consulting and services company optimizing drug development…

Drug Abuse Potential: A Data Analysis Strategy for Nonclinical Self-Administration Studies, New Webinar Hosted by Xtalks

Drug Abuse Potential: A Data Analysis Strategy for Nonclinical Self-Administration Studies, New Webinar Hosted by Xtalks

If a drug compound (or its metabolites) crosses the blood-brain barrier, then the FDA requires an Abuse Potential Assessment, which includes GLP self-administration, drug discrimination and physical dependency studies. For some drug classes like stimulants (i.e., amphetamine and cocaine), self-administration…

Assembling the eClinical Suite: Taking Advantage of the Latest Technology While Avoiding Vendor Lock-Ins, New Webinar Hosted by Xtalks

Assembling the eClinical Suite: Taking Advantage of the Latest Technology While Avoiding Vendor Lock-Ins, New Webinar Hosted by Xtalks

Not all eClinical applications are the same. For one thing, an eTMF, an EDC and a CTMS all fulfill different functions. Perhaps more importantly, they are all built with varying degrees of complexity. The eTMF and EDC are both relatively simple…

Next Generation Data Management Strategies for Clinical Trials, New Webinar Hosted by Xtalks

Next Generation Data Management Strategies for Clinical Trials, New Webinar Hosted by Xtalks

This live webinar upcoming on Friday, Nov. 16, 2018 at 11 a.m. EST (4 p.m. GMT/UK), will highlight how pharmaceutical companies like Karyopharm are employing new methods, business models and technologies for more effective data management outcomes in oncology. The discussion…

ESMO Update: State of the Art in Early Phase Oncology Trial Design, New Webinar Hosted by Xtalks

Aimed at small and mid-size companies with oncology assets, this one-hour webinar will present the theory behind early phase oncology studies, as well as the practical and logistical challenges to be prepared for when taking a compound into the clinic.…

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