Clinical Research
Our Approach
Founded in 2018, MR – Rheumatology Medicine was created with the mission of delivering excellence in patient care for individuals with rheumatic diseases, grounded in research, prevention, and comprehensive management.
Our clinical and research center is dedicated to providing the highest standards in the diagnosis and treatment of rheumatic conditions, with a multidisciplinary and cross-functional approach that ensures integration and effectiveness.
We remain committed to advancing scientific medicine and positioning ourselves as a benchmark in the field through quality, professionalism, and meaningful research.
For Researchers
Are you a researcher looking to join a team that values scientific insight and collaboration?
At MR, we share your commitment to clinical research. Let’s build the future of medicine together.
Our Pillars of Excellence
Efficiency
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Extensive regional experience in performance management, delivering tailored projects at both the national and international levels.
Regulation
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In-depth knowledge of local processes and comprehensive regulatory support to streamline approval timelines.
Quality
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Standardized and consistent processes that guarantee reliable outcomes across local and multinational settings, with transparency at every stage.
Monitoring
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Continuous oversight of clinical trials under ICH-GCP standards, with highly trained CRAs and experienced project managers, always prioritizing participant safety and well-being.
Drug Development Phases & Services
Drug Development Phases
Fase II
Evaluates preliminary efficacy and safety in selected patient populations.
Phase III
Confirms efficacy and safety across larger populations before regulatory approval.
Phase IV
Long-term follow-up and new indications after market approval.
Extension Studies
Gather long-term data following the primary study.
Observational Studies
Collect real-world data without direct intervention.
Post-study Analysis
Evaluate results and outcomes after protocol completion.
Core Services Throughout the Clinical Development Cycle
Regulatory Affairs
Comprehensive management of local and global compliance.
Patient Recruitment
Targeted support to achieve efficient enrollment.
Feasibility Assessment
Evaluation of resources and study viability.
Protocols & Strategies
Scientific and operational framework design for clinical research.
Clinical Trial Management
Coordination and oversight of all study activities.
Safety Management (SAE)
Documentation and reporting of serious adverse events.
Clinical Study Reports
Preparation of final reports for authorities and publications.
Audits & Inspections
Independent review to ensure regulatory compliance.
Compliance Monitoring
Continuous supervision to guarantee quality standards.
Risk Management
Systematic identification and mitigation of potential risks throughout the study lifecycle.
Clinical Monitoring
On-site and remote visits to ensure data accuracy, protocol adherence, and participant safety throughout the trial.
Legal Compliance
Fulfillment of ethical and contractual requirements.
Import & Logistics
Secure management of investigational products and clinical supplies throughout the supply chain.
Standard Operating Procedures (SOPs)
Standardized procedures ensuring operational consistency.
Vendor Qualification
Evaluation and approval of external providers and strategic partners.
Computerized Systems Validation
Review and validation of digital platforms to ensure data integrity.
