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Signant Biotech

The solution, the science and support all in one place

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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.

Experience matters

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We understand the importance of every trial, and every milestone, to emerging biopharma companies. As the leading evidence generation company with 25+ years’ experience, we’ve delivered from simple local trials to multinational pivotal studies. We've been there and back, and we're here to help.

NO DELAYS

Because every milestone matters, trust Signant to deliver high quality, on time, every time

NO DISCONNECTS

Trust Signant as your single partner for end-to-end eClinical technologies, scientific support, and mature, global operational delivery services that flow seamlessly

NO DOUBT

Rely on Signant to optimize your measurement strategy, deliver solutions tailored to your protocol, and deliver the highest quality clinical evidence

How we support clinical development for biotechs & emerging biopharma

Integrated platform

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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

On-demand expertise

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Supplement your team with clinical, scientific, and operational experts available in your time zone, reducing burdens on your team and facilitating smooth collaborations

Collaborative design

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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

Easy-to-use technologies

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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

7-1

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

8-2

Supplement your team with clinical, scientific, and operational experts available in your time zone, reducing burdens on your team and facilitating smooth collaborations

website - icons ss

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

website - icons - process

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

The solution, the science and the support all in one place

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

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Our Signant SmartSignals® Unified Platform is built with site-centricity in mind.  Easy to use, it contains all the eClinical components you need to optimize data collection and trial conduct for any study. It includes fully integrated EDC, eCOA, RTSM, eConsent, TeleVisits, and Participant Tracker applications which can be leveraged individually or together to meet the needs of your protocols..

Our Unified Platform ensures a streamlined experience for sites and sponsors:

  • All components are accessed through a single access point and using a single logon
  • All components are implicitly integrated, with no back-end data integrations needed.
  • Sites and Sponsors can move frictionlessly between all components (e.g., EDC, RTSM, eCOA, and eConsent) to complete their workflow.
  • The single study database enables efficient, consolidated oversight and reporting.

Ready in 4-6 weeks, leverage one or multiple components to drive your trial.

LEARN ABOUT UNIFIED PLATFORM
UNIFIED PLATFORM DEMO

A platform designed for biopharma

Streamline your clinical trials with Signant SmartSignals® Unified Platform. Discover how six fully integrated eClinical solutions optimize data quality and trial operations without extending lead times or complicating user experience. Perfect for emerging biopharma, our integrated suite is tailored to meet the unique needs of sponsors, CROs, and sites in a competitive landscape. Watch the video to learn more.

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

 
 

Want to learn more?

Learn how Signant Biotech accelerates & streamlines clinical development

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