DSP Clinical Research
Provider of outsourced clinical trial management and monitoring services with demonstrated focus on women’s health and reproductive endocrinology/infertility. Offers end-to-end and modular services spanning study start-up through regulatory submission, vendor management, data management, monitoring, and study rescue. Positions services with fixed-fee contracting and on-demand monitoring to support small- and mid-size sponsors.
Industries
Nr. of Employees
small (1-50)
DSP Clinical Research
Fairfield, Connecticut, United States, North America
Products
Medidata CTMS
A cloud-based, software-as-a-service (SaaS) clinical trial management system used by DSP Clinical to manage Phase I-IV clinical studies with flexibility and configurability for study-specific requirements.
On Demand Site Monitoring
A flexible, cost-effective monitoring service designed to fit the size, complexity, and speed of clinical research studies from Phase I–IV in any therapeutic area.
Comprehensive Clinical Trial Services
Services ranging from study startup through FDA submission including study start up, ongoing study management, multi-vendor management, site monitoring, study rescue/cleanup, site and monitor training & auditing, data management, statistics and medical writing, and FDA submissions.
Medidata CTMS
A cloud-based, software-as-a-service (SaaS) clinical trial management system used by DSP Clinical to manage Phase I-IV clinical studies with flexibility and configurability for study-specific requirements.
On Demand Site Monitoring
A flexible, cost-effective monitoring service designed to fit the size, complexity, and speed of clinical research studies from Phase I–IV in any therapeutic area.
Comprehensive Clinical Trial Services
Services ranging from study startup through FDA submission including study start up, ongoing study management, multi-vendor management, site monitoring, study rescue/cleanup, site and monitor training & auditing, data management, statistics and medical writing, and FDA submissions.
Services
Full-service trial support from study start-up through regulatory submission including study management, vendor coordination, monitoring, data management, statistics and medical writing.
Scalable monitoring support provided as needed to supplement sponsor or CRO teams, available for full-time or part-time engagement and deployable within approximately two weeks.
Provision and management of monitoring teams at lower cost than many staffing agencies or large CROs.
Assignment of an experienced study manager to oversee study conduct and manage vendors on behalf of the sponsor.
Modular outsourcing options to provide specific services (e.g., monitoring only, data management only) as required by the sponsor.
Full-service trial support from study start-up through regulatory submission including study management, vendor coordination, monitoring, data management, statistics and medical writing.
Scalable monitoring support provided as needed to supplement sponsor or CRO teams, available for full-time or part-time engagement and deployable within approximately two weeks.
Provision and management of monitoring teams at lower cost than many staffing agencies or large CROs.
Assignment of an experienced study manager to oversee study conduct and manage vendors on behalf of the sponsor.
Modular outsourcing options to provide specific services (e.g., monitoring only, data management only) as required by the sponsor.
Expertise Areas
- Clinical trial management
- Site monitoring and site management
- Women’s health and reproductive endocrinology/infertility
- Data management and EDC operations
Key Technologies
- Electronic data capture (EDC) systems
- SaaS Clinical Trial Management System (CTMS)
- Risk-based monitoring methodologies
- Clinical data management platforms
News & Updates
Case study documenting SaaS delivery of a clinical trial management system.
Article discussing risk-based monitoring approaches for smaller sponsors.
Article profiling the company in an industry publication.
Certified as a Women’s Business Enterprise by WBENC.
Named among the top 50 fastest-growing women-owned companies in North America.
Listed on Inc. 500 and Inc. 5000 fastest-growing privately held companies lists.
Case study documenting SaaS delivery of a clinical trial management system.
Article discussing risk-based monitoring approaches for smaller sponsors.
Article profiling the company in an industry publication.
Certified as a Women’s Business Enterprise by WBENC.
Named among the top 50 fastest-growing women-owned companies in North America.
Listed on Inc. 500 and Inc. 5000 fastest-growing privately held companies lists.