Empowering Global Healthcare
Clinterra
From Clinical Trials to Post-market safety, We protect patients while accelerating innovation
Who We Are
Decades of Safety & Clinical Excellence
With decades of experience across biotech, pharma, CROs, and digital health, Clinterra combines scientific insight with operational excellence. Our hybrid U.S.–EU model ensures both strategic leadership and efficient execution.
Core Capabilities
Integrated Clinical & Safety Services
Pharmacovigilance & Safety
– Safety leadership, ICSR review, signal detection, aggregate reports
Medical Monitoring
– Phase I-IV oversight, protocol review, trial compliance
Regulatory Affairs
– IND, NDA, MAA submissions, labeling, advisory board prep
Data Automation
– Argus integration, dashboards, NLP, automation workflows
Why Choose Us
Our experience in managing complex global clinical trials set Clinterra apart in the industry. With a focus on innovation, expertise, and a dedication to exceeding standards, we redefine the landscape of pharmacovigilance and clinical consulting services. By combining cutting-edge technology with a deep understanding of regulatory requirements, we lead the way in ensuring safety, compliance, and operational efficiency for our global clientele.
Let’s Connect
For inquiries or further information about our services, feel free to reach out to our dedicated team. We are here to assist you with any questions you may have regarding our pharmacovigilance and clinical consulting offerings. Your satisfaction and success are our top priorities, and we look forward to the opportunity to support your organization’s needs.
Phone: (617) 466-7896
Email: admin@clinterraglobal.com
Business Hours: Mon-Fri – 8am to 5pm
