What Does SureClinical Do?

    Learn about what SureClinical does, their services, and key information.

    What Does SureClinical Do?

    Name: SureClinical

    Headquarters: Reno, Nevada, United States

    Employees: 11-50 employees

    SureClinical is a software development company specializing in cloud-based clinical intelligence solutions for the life sciences industry. SureClinical delivers applications that automate, streamline, and accelerate the development and delivery of new drugs, therapies, and treatments to patients worldwide.

    Their primary offering is a unified platform designed to simplify and digitize clinical trial processes. By providing smart, rapid, and easy-to-use applications, SureClinical enables organizations to manage clinical documents, workflows, and collaboration securely and efficiently. The platform aims to reduce administrative burdens, improve compliance, and speed up the clinical development lifecycle for pharmaceutical, biotech, and clinical research organizations.

    Who Uses SureClinical?

    SureClinical serves a range of clients in the life sciences and clinical research sectors. Notable customers include Clinilabs Drug Development Corporation, First Coast Clinical Research, and Novotech. These organizations leverage SureClinical's platform to support clinical trial management and regulatory compliance.

    How Was SureClinical Started?

    SureClinical was founded by Zack, who brings over 20 years of experience in enterprise application development and product management from leading software firms such as Siebel, Oracle, and Adobe. Zack's background includes delivering technology products across industries, with a strong focus on pharma and life sciences, shaping SureClinical's approach to clinical software solutions. More details about their founding and leadership can be found on their About page.

    What Makes SureClinical Stand Out?

    SureClinical differentiates itself through its unified, cloud-based clinical intelligence platform, which is designed to be rapid to deploy and easy to use. Their focus on automation and streamlined workflows addresses the complex documentation and compliance requirements faced by organizations conducting clinical trials.

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