Signant Biotech Advancing medical discovery and innovation one program at a time. Download the Brochure Watch the Video Learn how Signant Biotech accelerates & streamlines clinical development Get from research to real world Biotech and emerging biopharmaceutical organizations drive innovations in healthcare through novel therapeutic discovery and development. But with many time-sensitive goals and priorities to manage, these clinical development programs need comprehensive solutions, on-demand expertise, and efficient resources to achieve research milestones. That’s where Signant can help. How we support clinical development for biotechs & emerging biopharma 1 On-demand expertise Supplement your team with clinical, scientific, and operational experts available in your time zone, reducing burdens on your team and facilitating smooth collaborations. 2 Collaborative protocol design Leverage our medical and clinical experts to assist in early protocol development and design, ensuring protocols are optimized to generate reliable data for any indication while simplifying participation. 3 Comprehensive technology, optimized to your study Drive accurate and reliable data, optimal site and patient experience, and simplified study management. Our fully integrated, unified platform of eClinical solutions will be customized to meet your study design quickly and cost-effectively. 4 Easy to use technologies Easy to use for sites and sponsors, our unified eClinical platform means single sign on, integrated data, and converged, guided workflow enabling users to move effortlessly between applications. Why partner with Signant Biotech for trial optimization? ONE PARTNER, MANY SOLUTIONS Work with one partner for end-to-end technologies, scientific support, and mature, global operational delivery services. ANY INDICATION OR TRIAL DESIGN Our nearly 25 years of experience means we are prepared and well-resourced to handle any study from simple, local trials to multinational pivotal studies. SPEED & COST-EFFECTIVENESS Engage us early to ensure you meet project and investment milestones on time and on budget. One integrated technology platform, tailored for emerging biopharma Signant Biotech is powered by Signant SmartSignals® Unified Platform which contains all the key technology components to optimize data collection and trial conduct for any study. It includes fully integrated EDC, eCOA, eConsent, RTSM, TeleVisits, and Participant Tracker applications which can be leveraged individually or together to meet the needs of your protocols. The unified solution ensures a streamlined experience for sites and sponsors: Single sign on Simpler, converged workflow across individual platform components A single database enabling efficient, consolidated oversight and reporting. Empower your study team with rapid implementation, using full-service or self-service models, so they can leverage the optimal solution to capture accurate data and run any trial efficiently. Backed by Signant Health expertise Science Study designs are supported by our experienced science team that ensures optimal design and industry best-practices. Logistics Our in-house logistics team prepares and distributes provisioned devices for all studies. Translations Our experienced team manages any new or adapted translations required, working with experienced, preferred translation vendors. Patient Helpdesk Patients can call our 24/7 multilingual helpdesk to gain help downloading or using our solutions. Scale Management Our experienced scale management team leverages relationships with instrument owners and authors to ensure current and approved versions are implemented. Scale Operational scale and global reach of Signant Health. Ready to Learn More or Get Started? Connect or Submit RFP
Biotech and emerging biopharmaceutical organizations drive innovations in healthcare through novel therapeutic discovery and development. But with many time-sensitive goals and priorities to manage, these clinical development programs need comprehensive solutions, on-demand expertise, and efficient resources to achieve research milestones. That’s where Signant can help.
Supplement your team with clinical, scientific, and operational experts available in your time zone, reducing burdens on your team and facilitating smooth collaborations.
Leverage our medical and clinical experts to assist in early protocol development and design, ensuring protocols are optimized to generate reliable data for any indication while simplifying participation.
Drive accurate and reliable data, optimal site and patient experience, and simplified study management. Our fully integrated, unified platform of eClinical solutions will be customized to meet your study design quickly and cost-effectively.
Easy to use for sites and sponsors, our unified eClinical platform means single sign on, integrated data, and converged, guided workflow enabling users to move effortlessly between applications.
ONE PARTNER, MANY SOLUTIONS Work with one partner for end-to-end technologies, scientific support, and mature, global operational delivery services. ANY INDICATION OR TRIAL DESIGN Our nearly 25 years of experience means we are prepared and well-resourced to handle any study from simple, local trials to multinational pivotal studies. SPEED & COST-EFFECTIVENESS Engage us early to ensure you meet project and investment milestones on time and on budget.
One integrated technology platform, tailored for emerging biopharma Signant Biotech is powered by Signant SmartSignals® Unified Platform which contains all the key technology components to optimize data collection and trial conduct for any study. It includes fully integrated EDC, eCOA, eConsent, RTSM, TeleVisits, and Participant Tracker applications which can be leveraged individually or together to meet the needs of your protocols. The unified solution ensures a streamlined experience for sites and sponsors: Single sign on Simpler, converged workflow across individual platform components A single database enabling efficient, consolidated oversight and reporting. Empower your study team with rapid implementation, using full-service or self-service models, so they can leverage the optimal solution to capture accurate data and run any trial efficiently.
Study designs are supported by our experienced science team that ensures optimal design and industry best-practices.
Our experienced team manages any new or adapted translations required, working with experienced, preferred translation vendors.
Our experienced scale management team leverages relationships with instrument owners and authors to ensure current and approved versions are implemented.