Clinical.ly offers a suite of software solutions, including eReg and eSource, designed to streamline regulatory compliance and document management for clinical research sites. By automating processes and enabling remote monitoring, their platform enhances operational efficiency, allowing sites to conduct more studies without increasing staff, resulting in a 3X to 10X improvement in workflow efficiency.
Funding
$1.1M 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
Clinical research sites face increasing regulatory burdens and rising labor costs, making it difficult to efficiently manage regulatory compliance and documentation. Traditional paper-based processes are time-consuming, prone to errors, and hinder remote monitoring capabilities, ultimately limiting the number of studies a site can conduct.
Solution
Clinical.ly offers a suite of software solutions designed to streamline regulatory compliance and document management for clinical research sites. The platform automates processes such as e-regulatory binder organization, document tracking, delegation logs, and training records. By digitizing and centralizing these functions, Clinical.ly enables remote monitoring by sponsors and CROs, reducing study initiation time and improving overall operational efficiency. The platform integrates proprietary workflows to remove barriers to adoption, allowing medical staff to focus on core responsibilities and conduct more studies without increasing staff.
Target Audience
Clinical.ly targets clinical research sites, including hospitals, academic centers, and private research facilities, as well as sponsors and CROs seeking to improve regulatory compliance and operational efficiency in clinical trials.
Features
- Electronic Regulatory (eReg) binder for streamlined organization and management of regulatory documents
- Electronic Source (eSource) for intuitive and efficient electronic source data capture
- ClinicallySign for purpose-built electronic signatures and document management
- Compliant electronic consent (eConsent) capabilities for a seamless consent experience
- ClinicallyPay for efficient study participant payments, improving retention
- Remote monitoring features enabling sponsors and CROs to access specified folders and logs
- Electronic delegation and training logs to ensure task delegation and training completion
- Integration capabilities with existing clinical trial management systems (CTMS) and electronic health record (EHR) systems