05.26.23 -- Make Your Clinical Trial Process More Efficient With Software And Services

This short video explains how and why business process outsourcing (BPO) using IQVIA Technologies for site payments offers excellent ROI for sponsors and peace of mind for sites and investigators.

OCT works with web-based data and provides full-service support through all phases of clinical development. We are dedicated to delivering high quality and accurate data within the desired timelines and tailored to sponsors’ specific needs.

Now operating as a fully integrated, unified platform with one user interface, Zelta has study sites in 109 countries and 60+ languages and dialects with more than 1.5 million electronic patient-reported outcomes generated through direct patient interactions.

Teams manually transcribing data often struggle with inefficiencies, time, and avoiding error. Discover OpenClinica Unite™, a powerful and easy way to leverage EHR data for clinical studies.

eClinicalGPS offers a variety of delivery models to fit any global payment process and structure. Learn how Greenphire's eClinicalGPS site payment solution offers flexible delivery models to maximize ROI, adoption, and help sponsors and CROs meet their business objectives.

This team of industry experts has extensive experience developing and delivering quality services for data management departments across all major therapeutic areas and phases for pharma/biotech companies. 

Medable's Total Consent offering, a fully enabled SaaS electronic consent management solution compatible with every clinical trial, is at the forefront of optimizing the informed consent process for potential trial participants by improving patient accessibility, knowledge, and experience.

With Medrio's combination of technology and consultative support from our team of experts, you can experience a seamless ePRO transition and establish a smoother path to regulatory submission.

Adoption of risk-based monitoring practices has grown in the industry of clinical trials at a slow but steady pace over the last decade. Examine some of the steps and operational challenges of onboarding central monitoring.

Mednet's EDC platform, iMednet, is user-friendly, customizable, and can be integrated with other clinical trial software, making it an ideal solution for clinical research teams looking to optimize their data management processes.

Watch how data linkage and tokenization at scale using Medidata Link effectively enables seamless integration into existing clinical workflows to provide linkage technology and capabilities for studies of any size and therapeutic area.

Curious about how to ease the patient and site journey? Improve your eCOA data collection and clinical trial efficiency with Kayentis and ClinOne's combined solution, covering eCOA, virtual visits, consent management, patient engagement, and more.

Sponsors, CROs, and sites are revolutionizing the way they collect electronic data from patients, physicians, and caregivers. Improve study start-up experiences with flexible deployment options, a groundbreaking global instrument library, and dedicated services and support.