Science focused
Bridging science and patients with integrity and innovation.
Professionalism
Collaborate with a CRO that values your expertise and supports your success.
Secure Support
We simplify regulatory and operational processes so you can focus on patient care.
Who We Are
Our Focus
1. Investigator-Initiated Studies (IIS)
Supporting clinicians and academic groups in designing, managing, and publishing independent research that advances medical practice.
2. Phase I–IV Clinical Trials
Providing full-service trial management — from early feasibility and safety studies to pivotal and post-market clinical investigations — across multiple therapeutic areas and device classes.
3. Real-World Evidence and Registries
Building and managing observational studies and registries that capture long-term outcomes, performance, and safety in real-life clinical settings.
4. Health Economics & Cost-Benefit Analysis
Generating robust economic data to support value-based healthcare decisions, reimbursement strategies, and comparative effectiveness studies.
5. Clinical Database Development
Designing secure, regulatory-compliant clinical databases that streamline data capture, monitoring, and analysis to ensure data integrity and audit readiness.
Our Advantages
• Investigator-Centric Approach
We understand the needs of clinicians and research teams, focusing on collaboration, flexibility, and scientific impact.
• Agile and Scalable Operations
Our structure allows us to adapt quickly to study complexity, timelines, and sponsor requirements.
• Regulatory and Quality Excellence
We maintain the highest standards of GCP compliance, data protection, and ethical conduct.
• End-to-End Expertise
From protocol design to publication, we manage every stage of the clinical research lifecycle.
Clinical Services
Clinical Trial Management
MD TRIAL provides end-to-end clinical trial coordination, supporting every phase of research — from protocol design and site selection to data lock and final reporting.
Our experienced project managers ensure that studies are delivered on time, on budget, and in full regulatory compliance, maintaining transparent communication with investigators, sponsors, and regulatory bodies throughout the process.
Regulatory & Ethics Support
Our regulatory affairs specialists manage all submissions to national authorities and ethics committees, ensuring compliance with GCP, MDR, ISO 14155, and local regulations. We assist in protocol and informed consent review, device classification, clinical evaluation plans, and communication with competent authorities to streamline study approval and execution.
Monitoring & Data Management
We offer comprehensive on-site and remote monitoring using a risk-based approach to ensure patient safety and data integrity. Our secure electronic data capture (EDC) systems provide real-time access to study data, supporting efficient query resolution, audit trails, and regulatory readiness.
Biostatistics & Medical Writing
Our biostatistics team delivers robust study designs, statistical analyses, and data interpretation that meet both scientific and regulatory expectations. We provide protocols, statistical analysis plans (SAPs), clinical study reports (CSRs), and peer-reviewed manuscripts, ensuring clarity, accuracy, and publication readiness.
Medical writers collaborate closely with investigators to translate complex results into compelling, evidence-based narratives.
Health Economics & Outcomes Research (HEOR)
MD TRIAL integrates health economics and real-world outcomes research to demonstrate clinical and economic value. We develop cost-effectiveness and budget impact models, conduct comparative effectiveness analyses, and generate evidence to support market access, reimbursement, and value-based healthcare decisions.
Collaborations and Partnerships
At MD TRIAL CRO, we believe that meaningful clinical progress happens through collaboration. We work closely with partners across the healthcare and research ecosystem to generate high-quality, practice-changing evidence that advances patient care and supports innovation.
Our network brings together clinical, academic, and industry expertise, ensuring that every study benefits from multidisciplinary insight and real-world applicability.
We collaborate with leading partners, including:
• University Hospitals and Specialized Research Centers
We partner with top-tier academic hospitals to conduct high-quality clinical investigations.
Our collaborations in investigational programs provide access to experienced investigators, diverse patient populations, and advanced clinical infrastructure.
• Medical Device Manufacturers
We work with innovative medtech companies — from early-stage developers to global manufacturers — to design and execute post-market clinical studies.
We help industry partners generate regulatory-grade evidence, optimize cost-benefit strategies, and build real-world datasets to support market access and product differentiation.
• Academic Institutions and Professional Societies
We maintain active collaborations medical societies, supporting investigator-initiated studies, registries, and consensus-driven research programs.
These partnerships foster scientific exchange, methodological rigor, and the dissemination of results through high-impact publications and conference presentations.
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