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news roundup
Bio-Optronics and Synexus announce partnership aimed at improving patient access to modern medicine and clinical trial efficiency by delivering high numbers of quality patients to clinical trials through the use of a unified CTMS across the entire Synexus network of more than 200 sites in eleven countries worldwide.
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Bridging Clinical Research & Clinical Health Care – Let’s Build a Bridge
The Bridging Clinical Research & Clinical Health Care Collaborative, April 4-5, is the only forum that brings together representatives from clinical research, health care, regulatory agencies, patient advocacy groups and academia to envision a true collaborative solution to build a bridge between clinical research and health care.
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ERT announced it has launched a certification program for Phase I investigative sites conducting cardiac safety studies. This program trains sites to collect precise cardiac safety data by using ERT’s proprietary Expert Precision QT approach so that trial sponsors and CROs can determine the safety of their compounds earlier in development.
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Protein Biotherapeutic BioAnalysis, by Immunoaffinity LC-MS: Latest Trends and Recommendations
Live Webcast: Tuesday, May 15, 2018
11am EDT | 8am PDT
4pm BST | 5pm CEST
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Six CROs and Veeva Systems introduced Align Clinical CRO, a new industry standards group dedicated to making it easier for sponsors and CROs to work together during clinical trials through the improvements of trial execution and collaboration with life sciences companies.
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Where Expertise Meets Nuance: Conducting PTSD Clinical Trials
Live Webcast: Tuesday, April 24 at 11:00am EDT
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WIRB-Copernicus Group Clinical Services Division announced its acquisition of ACI Clinical, a provider of Endpoint Adjudication and Data Monitoring Safety Committees. ACI Clinical will provide a committe of experts for WCG's clients in order to support their decisions around clinical development programs.
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Move Your Immuno-Oncology Therapy Forward in 2018 and Beyond
Live Webcast: Thursday, April 5 at 11:00am EDT
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Scientific Advice with Regulators – An Essential Tool in Early Drug Development
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Patient-Centric Complex Trial Design & Site-Less Visits: How Study Design & IRT Can Ease Patient Burdens
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Articles
There are many benefits for sites adopting electronic informed consent and it is vital that site study teams are not bystanders in the move towards its use.
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Managing the Placebo Problem in Chronic Pain Studies
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Rho offers their expertise on why it is important to have a pre-IND meeting to ensure a successful IND.
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PV Research Reveals Momentum Towards Cloud and AL
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Blog Posts
Building upon the usage of technology in health care delivery, integrating technology into clinical research as a care option will be a game changer in achieving greater participation in clinical research and decreasing the overall time for trial completion.
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The Benefits of a Data-driven Approach to Feasibility
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To encourage experimentation with more complex clinical trial strategies, FDA plans to launch a pilot program to assess complex studies proposed by sponsors.
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Achieve Better Early Clinical Development Outcomes - Faster
Use existing global network site relationships for improved early phase quality, costs and timelines
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