Pre-IND Program Evaluation and Development, Clinical Development Planning, Pre-IND meetings, IND services and filings, Phase I - IV Program Development and Management, Protocol Design, Intelligent CRF Design, Scientific and Medical
Writing Services, Strategy and Design Meetings with Regulatory Agencies, Pre-Launch Activities, Investigator Meetings, Focus Groups, Branding & Positioning Activities, Drug Development Business Model Deployment, IRB Management, Contract & Grant Negotiation and Management Services, Clinical Trial Instructional Assistance, Opinion Leader Modeling and Positioning.

Synergy can independently manage and monitor your clinical trial, or work  as a team with the sponsor's team as a true extension of existing research personnel.  We have and are conducting clinical protocols in over 300 US centers, as well as 30 international research institutions.  Foreign protocols include France, Russia, Germany, Israel, and Canada.

Synergy places a great emphasis on the use of state-of-the-art technologies to facilitate clinical trial management and monitoring.  Speak to us about real-time monitoring strategies that can save time and money for your program.