Pharmaceutical, biotechnology and medical device manufacturers, and companies conducting clinical trials continually look for more effective ways to manage their clinical operations and ensure product safety. They look for mature yet innovative technologies to meet their data and safety management needs and, ultimately, to reduce time-to-market in an industry where accelerated product delivery can translate into billions of revenue dollars.

Since 1997, Phase Forward has played a pivotal role in developing and delivering industry proven solutions for electronic data capture (EDC), clinical data management (CDM), and drug safety monitoring and management. Our integrated product portfolio provides the end-to-end functionality – and the level of reliability and scalability – that customers of all types and sizes need when developing and delivering new drugs and medical devices in a highly regulated, continuously evolving market.


Through our active participation in standards organizations, and our ongoing commitment to meeting the high-quality standards of Good Clinical Practice, we help ensure that customers remain up-to-date with compliance and regulatory-related issues.


To date, our products and services have been used in over 10,000 clinical trials involving more than 1,000,000 clinical trial study participants at over 290 life sciences companies, regulatory agencies and non-profit organizations worldwide.

Clinical Data Solutions

Learn more about our comprehensive clinical data solutions:

Phase I Clinic Automation

Learn more about our phase I automation solutions:

Safety Solutions

Learn more about our pre-marketing and post-marketing safety solutions: