ClinDatrix is Different

ClinDatrix is a CRO serving the pharmaceutical, biotechnology and medical device industries globally. We provide world-class performance and quality at a moderate price.

See Why ClinDatrix is Different

Services

From our inception, the ClinDatrix vision has been to offer comprehensive, world-class CRO services to innovators in the pharmaceutical, biotechnology and medical device industries. Through our U.S.-based staff and global affiliates, we are a trusted choice for firms conducting Phase I-IV trials domestically or around the world.

Our core strengths enable us to guide our clients so that their studies yield accurate, reliable data. Our workflow processes and procedures are governed by a full suite of SOPs that are compliant with GCPs and ICH and FDA guidelines. We utilize advanced equipment and systems including Oracle InForm for global electronic data capture (EDC). All of our GxP systems are fully validated and managed using change control.

Everything ClinDatrix does, from protocol review and CRF design to clinical study reports and regulatory submissions, helps advance our clients along their product development pathways.

Clinical Trial Project Management

Clinical Trial Investigator Meetings & Event Planning

Clinical Monitoring Services - CRO Irvine Orange County

Clinical Trial Monitoring

Clinical Trial Medical Monitor & Medical Safety

Clinical Trial Data Management

Clinical Trial Biostatistics

Medical Writing Services

Quality Assurance for Clinical Trials

Clinical Regulatory Affairs

How ClinDatrix is Different...

ClinDatrix is very strong in technology and can use its mastery of on-premise systems to deliver results faster. For example, an EDC database can be built in 5 weeks instead of 12 weeks.

We invest a lot in our support. We keep our extensive arsenal of how-to’s and help docs regularly updated, and if you have a set-up question, we are here to chat. Everything ClinDatrix does, from protocol review and CRF design to clinical study reports and regulatory submissions, helps advance our clients along their product development pathways.

Core Strengths

We guide our clients with clinical project management and data management so that their studies yield accurate, reliable data. Our workflow processes and procedures are governed by a full suite of SOPs that are compliant with GCPs and ICH and FDA guidelines.

Equipment & Systems

We host on our servers Oracle InForm for global electronic data capture (EDC). Hosting InForm on our servers allows us to set up a study database in 5 weeks versus 10-12 weeks in the cloud.

Fully Validated

All of our GxP systems are fully validated and managed using change control.

Leadership

ClinDatrix leverages the successful career experience and extensive knowledge of its founders, Louise M. Murphy, President and CEO, and Brian G. Murphy, CFO and Chairman of the Board, to advance our clients’ clinical research.

Today the firm employs an executive management team whose members each have an average of 20 years of industry experience and 10 advanced degrees among them. Utilizing the team’s strong project management skills and expertise honed by hands-on experience, ClinDatrix works in partnership with our clients to deliver excellent contract research services.