Acceliant offers eClinical trials solutions to global contract research organizations, pharmaceutical and medical device enterprises
Acceliant is a preferred partner of global contract research organizations (CROs), pharmaceutical and medical device enterprises for e-Clinical trials solutions and services. Our journey coincides with the origin of the e-Clinical trials industry. Our expertise and long-term relationships with sponsors help us shape the next-generation e-Clinical suite of solutions.
“Acceliant is a young and dynamic organization with a proven track record of innovation and creating a robust and integrated platform for clinical data management ”
Advantage Acceliant
Healthcare first
Acceliant has the mindset of a healthcare enterprise. Our intimate understanding of the healthcare industry helps us intuitively address the diverse clinical trials needs of CROs, pharmaceutical companies, and medical device manufacturers. Our experienced team develops healthcare solutions that cater to the requirements of constituents, including patients, regulators, and payers.
Powered by technology
Acceliant uses new and emerging technologies to deliver sophisticated eClinical trials solutions and services. Our suite of solutions is hosted on the cloud, offering variable scalability and cost benefits across the clinical trials lifecycle. We partner with Amazon Web Services and Microsoft Azure, the leaders in on-demand cloud computing. Our solutions provide enterprises with the convenience of a mobility advantage.
Time-to-market
Acceliant accelerates outcomes during clinical trials by blending process rigor with robust technology. We reduce the design process of case report forms (CRFs) from months to weeks with a proprietary clinical trials design platform. Our drag-and-drop interface and one-click functionality streamline clinical trials. We undertake deployment and training in less than two weeks, significantly reducing your clinical trials costs.
Global platform, local needs
Acceliant’s eClinical trials platform is a universal solution that can be customized to meet the specific needs of sponsors. It complies with Clinical Data Interchange Standards Consortium (CDISC) standards, the United States Food and Drug Administration (FDA) Code of Federal Regulations (CFR) 21 Part 820 and the International Organization for Standardization (ISO) 13485:2003 guidelines for medical devices. Our platform has been certified for use in multiple languages, including English, Japanese, Mandarin, and Spanish.
Our achievements
Life sciences is not something we do, it’s everything we do! It's our DNA.
100+
Clients
400+
Global submissions