Individual products that meet your needs today. A connected platform that is ready for you to grow into.
Navigate compliance and reduce risks throughout your clinical trial with our experts at your side.
Enhance clinical trial efficiency and power global studies with the industry leader in practical, eClinical innovation. Simplify and automate clinical processes around the world.
Streamline clinical research from site identification to study closeout with seamlessly connected solutions and services that support your success.
Navigate the ever-evolving global regulatory landscape with technology and services that ensure compliance, mitigate risk, and avoid costly delays.
Simplify quality control across your clinical content, processes, and training with scalable and comprehensive quality solutions.
Reduce IT burdens throughout your study with technology that meets usability, scalability, performance, validation, connectivity, and security requirements.
Corrective and Preventive Action (CAPA) management is a cornerstone of quality and compliance, but many CROs and site teams struggle to know where to begin. With the recent updates to GCP guidelines, ICH E6(R3), now is the time to ensure your CAPA process is risk-based...
Library
Webinar
Trust the Process - TMF Document Submission Considerations
Breaking Silos: Enhancing Cross-Functional Collaboration in TMF Management
Quick Guide
A Guide for Best Practices with Sponsor Oversight
Trust the Process - The Move from Paper to Electronic TMF
Mobile eTMF: Once a “Would-Be-Nice”. Now a “Must-Have”!
Consolidating Your Language Outsourcing
FDAAA: Considerations to Limit Expenditures
Moving Towards Electronic Clinical Trials
The Path of Resistance
Experience with eTMF and Site Archiving
Global Call Centers for Life Sciences Organizations
Freeing Up Investigators' Time to Engage with Patients
Engage With Patients, Not Paper
Resourceful Resourcing: Consolidate Your Tech Providers
eTMF: Yes, Virginia, Paper is Disappearing
Paperless Clinical Trial Optimization
Mid-Study Transition of a Global Study
Running A Paperless Clinical Trial
Correlation: Patient and Clinical Reported Outcomes
The Pharmacovigilance System Master File
4 Ways You Can Overcome Roadblocks to Tech Adoption
Leverage Clinical Data to Streamline Global Development
A Holistic eClinical System
Streamline Your Global Pharmacovigilance Management
