Signant Health Launches Signant Biotech
Signant Health has announced the launch of Signant Biotech—an integrated clinical research approach leveraging software and services tailored to the unique needs of small- to mid-sized biopharmaceutical organizations.
Signant Biotech is anchored by a unified technology platform consisting of fully integrated EDC, eCOA, eConsent, RTSM, and telemedicine solutions. Delivered in conjunction with Signant's scientific and regulatory expertise, the technology platform and accompanying services enable customers to scale from local to multinational studies.
Studies using the unified platform can be implemented in typically four to six weeks. Sponsors and contract research organizations (CROs) can also elect to deliver studies using a self-service model. Either approach is enabled by a configurable designer tool that allows non-technical staff to build studies without software coding. The designer leverages a library of pre-built forms and edit checks which further accelerates study builds.
"We know that small- to mid-sized biopharma sponsors have unique needs," said Graciela Racaro, chief operating officer of Signant in a press. "They want to work with a partner who can balance flexibility and standards to get them to their readouts as quickly and efficiently as possible. They also want to leverage a partner's experience and lessons learned from similar trial designs and global launches."
"We appreciate that our smaller customers in the biotech segment are in a challenging funding environment, where money comes less easily and at more expense," said Roger Smith, chief executive officer of Signant Health in a press release. "We are pleased to support this segment of customers with technology and services that allow them to focus their precious time and resources on advancing their clinical assets, and not having to make trade-offs between scale, capability, accountability, and value."
Reference
Signant Health Launches Signant Biotech to Accelerate and Streamline Clinical Development for Emerging Biopharmaceutical Organizations. (2023, October 3). Cision PR Newswire.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
