Clinical Research

Projecis meets the unique needs of the clinical research industry by addressing how people and content are assigned and logged within the system, allowing for precise analytics, simplified process, and timely trial completion. Developed by a professional in the industry, Projecis solves the needs of today's clinical research teams.

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	Assign specific industry roles to create a history of your projects, as well as precise project metrics. Bring your entire team to Projecis — sponsors, sites, CROs — and assign roles including Data Manager Clinical Research Associate (CRA), Principal Investigator, Medical Writer and Statistician.
	Create project specific qualifications for member profiles (e.g., certifications, training logs) accessed in document form for easy review by quality officials to determine team member function and role.
	Implement blinding with security features on both a company and individual-level, allowing for more robust "double-blind" situations.
	Project artifacts can be tagged with common industry categories for ease of reference and search. Categories include Safety, Protocol, Programs, Regulatory and Submissions.
	Access disparate clinical project databases , including interactive voice-response (IVR), electronic data capture (EDC), and safety surveillance in one place. Get automated news reports, milestone alerts, and specific data points. Tracking and reporting is monitored with patient enrollment, serious adverse events (SAEs) and cross-database checks.
	Projecis is compliant with 21 CFR Part 11 regulations and can assist with efforts to comply with study and industry regulations.