INSIGHTS ON CLINICAL TRIAL PARTNERING
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4C Pharma Harnesses CRO Expertise With A Unified Platform
A pharmacovigilance company with abilities in case processing, MICC, regulatory and medical writing turned to Oracle seeing them as the gold standard.
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Think Canada: The Team Behind Your Clinical Trials
Altasciences has a bioanalytical and clinical facility in Canada. In this video, we unveil the advantages of conducting trials in Canada while introducing some of the faces that work behind the scenes on your studies.
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Best Practices For Site Selection & Study Startup
Learn how by addressing study startup challenges head-on and fostering effective teamwork, researchers can optimize process efforts, setting a solid foundation for the research endeavor's overall success.
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AMR Shares How SIP Has Transformed Their Clinical Trials
Missy MacPhail, Executive Director of Business Development at Alliance for Multispecialty Research, LLC shares her experience with SIP and how it's benefited AMR.
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Canadian CTA Frequently Asked Questions2/20/2024
This FAQ list offers clarity on pivotal aspects of your drug development journey, ensuring studies in Canada pave the way for U.S. FDA and EMA submissions.
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Clinical Trial Logistics: Meeting Unique Participant Needs2/16/2024
Uncover why delivering a comprehensive service entails establishing a robust global network equipped with the expertise, resources, and adaptability to address diverse participant needs worldwide.
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Partnering With An Integrated CRO/CDMO: 5 Things You Need To Know1/9/2024
Sponsors always ask, “Will the partnership save me time and money?” and “How can you streamline the complex development processes for me?” Get the answers to these questions and more.
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The Advantages Of Outsourcing IRB And IBC Reviews To One Partner8/30/2023
To streamline reviews, learn how sponsors can coordinate both IBC and IRB assessments through a vendor offering integrated resources.
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Too Many Trials, Too Few CRAs: Closing The Capacity Gap9/16/2022
The clinical trial industry has experienced 5.8% annual growth year over year–but the growth in CRAs and research sites isn’t keeping up. Read on to learn how these capacity gaps can be closed.
CLINICAL TRIAL PARTNERING SOLUTIONS
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Delve into how this partner's scalable packaging services for logistics support can achieve higher operational efficiency and lower quality and safety risks.
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Ready to make your research altogether better? Learn how Advarra® is assisting clients to reduce risk and ensure adherence to good manufacturing practice (GMP), good laboratory practice (GLP), and good tissue practice (GTP) standards.
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Whether it's complex randomization, adaptive trials, Direct-to-Patient models, or recurring visit cycles, discover how Rave RTSM is able to grant your team instant access to the full spectrum of current and forthcoming study features.
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Grasp how the Medidata Clinical Cloud® is able to streamline setup and operation, operate comprehensive and adaptable supply controls, eradicate the need for reconciliation, minimize potential risks, and more.
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Clinical teams are responsible for driving trial timelines during the study start-up phase of any study. Unearth how Florence SiteLink is able to create a digital link between teams and their sites.