Newsletter | May 26, 2023

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

The ROI Of IQVIA Site Payments

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.

Your Clinical Study Data Is In Good Hands

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.

New Name, Same Great Experience – Meet Zelta

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.

So Long, SDV! Experience Automated Source Data Capture's Speed & Safety

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 Site Payment Solution

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.

Proper Data Management Across All Areas & Phases

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 Total Consent: The Future Of Informed Consent

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.

The Medrio Electronic Patient Reported Outcomes Platform

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.

Central Monitoring: First Steps To A Risk-Based Approach

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.

Accelerate Study Start-up With iMednet’s Flexible EDC

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.

The Future Of Clinical Development: Implementing A Scalable Data Linkage Strategy

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.

Improve eCOA Data Collection And Clinical Trial Efficiency

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.

Cut Study Start-Up Times By Up To 50% With eCOA

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.