Yaoyanshe is a clinical research organization (CRO) technology platform that connects global pharmaceutical companies with local clinical research partners, streamlining the entire process from regulatory consultation to project delivery. By enhancing collaboration and ensuring quality across all stages, the platform reduces costs and accelerates timelines for clinical trials in the medical industry.
Funding
$86.2M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Global pharmaceutical companies face challenges in efficiently connecting with reliable local clinical research partners, leading to increased costs and prolonged timelines for clinical trials. The complexities of navigating regulatory landscapes, selecting appropriate sites and investigators, and ensuring quality collaboration across different stages of the research process further exacerbate these issues.
Solution
Yaoyanshe offers a technology platform designed to streamline the connection between global pharmaceutical companies and local clinical research organizations (CROs) and site management organizations (SMOs) in the Asia Pacific region. The platform provides a one-stop trading solution that manages the entire clinical research process, from initial regulatory consultation and project investigation to site and investigator selection and project delivery. By ensuring quality collaboration and seamless link management, Yaoyanshe aims to reduce costs, accelerate timelines, and improve the overall efficiency of clinical trials. The platform also offers tailored trading experiences with enhanced protection and support to facilitate business growth.
Target Audience
The primary target audience includes global pharmaceutical companies seeking to connect with local clinical research partners in the Asia Pacific region, as well as CROs and SMOs looking to expand their network and access new projects.
Features
- Seamless linking of regulatory consultation, project investigation, site selection, and CRO/SMO management.
- Quality assurance mechanisms to ensure effective collaboration between clinical research partners.
- Curated benefits such as enhanced protection and extra support for business growth.
- Support for various clinical research supplier groups, including market investigation, steer committees, medical imaging, and central laboratories.
- Compliance with ISO 27001, ISO 9001, and ISO 27701 standards, ensuring information security, quality management, and privacy information management.