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news roundup
Updated employee announcements, business news, awards, and recognition in the industry today.
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Speed, Efficiency and Accuracy in Site Contracts and Payments
Negotiating investigator site contracts and budgets, coupled with delivering global investigator payments, can be challenging. By coordinating services to work together cohesively, the clinical trial process can be streamlined. Download this Executive Summary for an expert discussion on expediting the delivery of global clinical trial contract negotiation.
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The European Medicines Agency’s Management Board met to discuss EMA’s future premises in Amsterdam.
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Considerations for Efficient Site Contracts and Payments
Clinical trial agreement development has a tremendous impact on study start-up – integrating site-level budgets, payment terms, and Clinical Trial Management Systems set-up. By understanding the most important considerations for contract development and budget planning, you can execute a fully-integrated process that results in high-efficiency enabled contracts and payments.
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Bio-Optronics announces the release of an advanced business intelligence reporting module designed to provide health systems, CROs, and other research organizations real-time access to analytics.
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Scientific Advice with Regulators – An Essential Tool in Early Drug Development
Live Webcast- Europe: Thursday, March 29, 2018 at 3:00pm CEST, North America: Tuesday, April 17 at 11:00am EDT
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Medrio, Inc. has announced the company’s international and domestic channel expansion, which includes EMEA and APAC. With the expansion will come five new offices and a new business development team made up of a Vice President, Senior Director, and Managing Director.
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The Benefits of a Data-driven Approach to Feasibility
Live Webcast: Tuesday, March 20 at 11:00am EDT
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Articles
The FDA’s new draft IVD Guidelines will need to be factored into how pharma clinical trial sponsors use IVDs in a clinical trial, study design, timeline for protocol development, IND submission, and study initiation.
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Immuno-Gene Therapeutics in Hematological Cancers: How Science Drives Study Strategy
Live Webcast: Tuesday, February 20 at 11:00am EST
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Numerous factors can adversely impact study startup and its efficiency, in an industry plagued by rising development costs and increasing complexities.
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Blog Posts
In this interview, Jennifer Prichard, MD, Medical Monitor at Atlantic Research Group, and Hunter Walker, CTO at Atlantic Research Group will discuss challenges with existing medical monitoring processes, and how new technologies can help improve efficiency.
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The Rare Disease Revolution
On Demand
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The 10th anniversary of the Clinical Trials Transformative Initiative provided an opportunity for FDA officials to join with study sponsors and research experts to examine the policy achievements and plans for future efforts of improving clinical trials.
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