Services
Acceliant offers a suite of clinical trials solutions for contract research medical device enterprises
Acceliant understands the context that our sponsors operate in to deliver customizedclinical trials solutions. We combine people, process, and technology to deliver bespokesolutions for contract research, pharmaceuticals, and medical device enterprises. Acceliant aligns a robust suite of solutions and governance mechanisms to meet the unique needs of enterprises. Our healthcare DNA enables us to empathize with the diverse requirements of constituents and stakeholders during the clinical trials journey. Our solution approach has made Acceliant the preferred clinical trials partner of global sponsors.
Acceliant understands the context that our sponsors operate in to deliver customizedclinical trials solutions. We combine people, process, and technology to deliver bespokesolutions for contract research, pharmaceuticals, and medical device enterprises. Acceliant aligns a robust suite of solutions and governance mechanisms to meet the unique needs of enterprises. Our healthcare DNA enables us to empathize with the diverse requirements of constituents and stakeholders during the clinical trials journey. Our solution approach has made Acceliant the preferred clinical trials partner of global sponsors.

Usability advantage
Acceliant uses design thinking to enhance the usability of clinical trials. Our platforms and solutionsfocus on a patient-friendly experience to harness data. Our clinical trials ensure that patients, processes, and technologies are integrated to deliver seamless clinical outcomes. Acceliant is recognized for usability by independent global industry bodies.

Cloud advantage
Acceliant was one of the early adopters of the cloud for clinical trials. Our suite of clinical trials solutions is hosted on the cloud, providing you the flexibility to ramp up trials and access clinical data anywhere, anytime. Our technologistshave established a stringent data and information security policy to ensure data integrity, redundancy, and risk mitigation during and after clinical trials.
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