Welcome to CRI we are leading Clinical Research Site Management Organization (SMO) dedicated to facilitating high-quality clinical research. As your trusted partner, we specialize in optimizing the operational efficiency of clinical trials, ensuring seamless execution from initiation to completion. Our therapeutic areas include Oncology, Cardiovascular, Respiratory, Diabetic, Infectious disease, Dermatology, Orthopedic, Psychiatry, etc
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services
services
Provide Quality clinical research strategy and monitoring for Pharmaceuticals products, nutraceuticals, biological products and medical devices as per regulatory requirement
Early Phase Clinical Development (Phase I Trial)
Bioanalytical Services
Pharmacovigilance Services
Regulatory Services Bioavailability & Bioequivalence studies: End to end BA/BE study development and execution (Pilot & Pivotal)
Late Phase Clinical Development (Phase II, Phase III & Phase IV Trials)
Clinical Data management & Biostatistics services
SMO Services
Site Selection & Activation
Site Selection & Activation
Leveraging our extensive network, we identify optimal sites for your clinical trials and streamline the activation process
Study Management
Study Management
Our experienced team oversees all aspects of study conduct, including patient recruitment, regulatory compliance, data collection, and site performance monitoring, ensuring adherence to protocol requirements.
Quality Assurance
Quality Assurance
We implement robust quality assurance measures to uphold the integrity and reliability of clinical trial data, conducting regular audits and inspections to maintain compliance with regulatory standards.
Patient-Centric Approach
We prioritize the needs and well-being of study participants. Our patient-centric approach ensures that clinical trials are conducted with the highest ethical standards and respect for human dignity.: We prioritize the needs and well-being of study participants.
Patient Engagement
Patient Engagement
Through targeted outreach and engagement strategies, we enhance patient recruitment and retention, fostering positive relationships between investigators and study participants
Regulatory Expertise
Regulatory Expertise
Navigating the complex landscape of regulatory requirements can be daunting. Our team of regulatory experts provides guidance and support to ensure compliance with local and international regulations, minimizing regulatory delays and ensuring smooth study execution.
Continuous Improvements
Continuous Improvements
We believe in continuous improvement and strive to enhance our processes and services continually. Through feedback mechanisms and performance metrics, we identify areas for optimization and implement proactive measures to drive efficiency and quality in clinical trial operations
Data management
Data management
Data is the backbone of clinical research. Our advanced data management solutions ensure accurate and reliable data collection, storage, and analysis, enabling informed decision-making and timely study outcomes
Milagro Clinical Research Organization (CRO Partner)
As a CRO Partner Milagro Provides integrated trial solution as well as specific service components based on sponsor need
High-quality services and expertise whether you need a full service model are only specific service offerings
Established relationships with trusted verified partners and vendors.
A comprehensive, ongoing training program to ensure consistent competent service delivery with a focus on quality
Seamless integration with your team and study sites, regarding of location or time zone.
Flexibility, innovation, and creativity to meet your study development and execution needs with a collaborative approach.
A stable team with longevity most of our staff have been with us for years
Many domestic and international sponsors have entrusted us to manage hundreds of clinical trials either providing full or selected services
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