“Accelerating Innovation. Advancing Global Health.”

NEOREX CRO is your trusted global partner for full-spectrum clinical research services. We support pharmaceutical and medical device companies with scientifically driven, ethically grounded, and regulatory-compliant solutions across all phases of clinical trials.

"Empowering Clinical Breakthroughs."

From protocol design to patient recruitment — we deliver results that accelerate therapies to the people who need them most. With unmatched regional expertise and a global outlook, NEOREX CRO bridges science, strategy, and execution.

"Science with Integrity. Trials with Impact."

We don’t just run trials — we ensure every milestone is met with transparency, compliance, and care. At NEOREX CRO, our scientific advisory board and expert team bring decades of experience to every project.

"Global Reach. Local Strength."

Wherever your trial goes, we’re already there. With a rapidly expanding global site network and deep local knowledge, NEOREX CRO ensures your study is in the right hands — from startup to closeout.

NEOREX CRO

Welcome to NEOREX CRO, where innovation meets operational excellence in clinical research. With a strong foundation in science and a global outlook, we help pharmaceutical and medical device companies accelerate their clinical development programs. Whether you're initiating a new study or expanding your trial portfolio, our team delivers tailored, high-quality services that combine clinical expertise, regulatory insight, and operational precision.

  • Comprehensive Global Clinical Trial Support
  • International Reach with Local Expertise
  • Scientific Board of Therapeutic Area Leaders
  • Transparent, Ethical, and Compliant Operations
  • Expansive Site Network and Site Relationships

Hematology

Hematology

We manage complex trials in non-malignant and malignant hematologic conditions, including anemia, bleeding disorders, and hematologic cancers. Our scientific board provides input into biomarker strategies and emerging treatment modalities.

Cardiology

Cardiology

We provide strategic and operational support for trials involving heart failure, ischemic heart disease, arrhythmias, and cardiovascular devices. Our board-certified cardiology experts ensure clinical relevance and protocol integrity across all phases.

Oncology

Oncology

Our oncology experts bring extensive experience in solid tumors, hematologic malignancies, immunotherapies, and targeted agents. We support early- and late-phase oncology trials with rigorous safety monitoring, scientific oversight, and tailored recruitment strategies.

Infectious Diseases

Infectious Diseases

From antimicrobial resistance studies to global vaccine trials and viral therapeutics, our team supports trials aligned with current public health priorities and emerging infectious threats. Scientific input supports both trial design and safety oversight.

Internal Medicine

Internal Medicine

With a broad scope covering chronic diseases, metabolic disorders, and multi-system conditions, our internal medicine advisors help ensure cross-disciplinary trial planning and execution for studies involving complex patient populations.

Core Services

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CRO Services for Medical Device Trials

  • Full-service support for medical device clinical investigations
  • Compliance with MDR/IVDR regulations and ISO standards
  • Expertise in device trial design, execution, and documentation
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Protocol & Training Services

  • Protocol development in collaboration with our scientific board
  • Site and investigator training in GCP, study procedures, and compliance
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Clinical Operations Consultancy

  • Tailored consulting for operational planning and study design
  • Support for market entry and regional expansion strategies
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Medical Monitoring & Safety Oversight

  • Medical oversight from experienced physicians and specialists
  • Pharmacovigilance and adverse event management
  • Ongoing safety data review and analysis
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Study Start-Up Services

  • Contract and budget negotiations
  • Regulatory document collection and submission
  • Site initiation and pre-study visits
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Feasibility & Site Selection

  • Data-driven feasibility assessments
  • Strategic site selection 
  • Collaboration with investigators to optimize trial success
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Site Relationship Management

  • Development and management of a high-performing site network
  • Relationship building with investigators and institutions
  • Site training and continuous engagement
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Licensing Services

  • Product registration and marketing authorization support
  • Dossier preparation and submission in accordance with local and international regulations
  • Regulatory pathway consulting for pharmaceuticals and medical devices
  • End-to-end coordination with regulatory authorities for licensing success
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Regulatory Affairs

  • Regulatory strategy and submissions (local and global)
  • Ethics committee and ministry approvals
  • Regulatory intelligence and compliance support
  • Support for both pharmaceutical and medical device regulatory requirements
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Clinical Trial Management

  • Full-service management of Phase I–IV clinical trials
  • Site selection, initiation, and close-out
  • Investigator and site coordination
  • Patient recruitment and retention strategies
  • Risk-based monitoring

Why NEOREX?

Choosing the right partner is critical to the success of your clinical development program. At NEOREX CRO, we don’t just offer services — we deliver strategic partnerships grounded in scientific rigor, operational excellence, and unwavering commitment to quality.

What Makes Us Different

Let’s Advance Together

At NEOREX, we are more than a service provider — we are an extension of your team. Our goal is to help you bring innovative therapies and technologies to patients safely, efficiently, and successfully.

Contact Us

Let’s Talk About Your Next Clinical Milestone.

Whether you're planning a new clinical study, exploring regulatory pathways, or seeking a strategic CRO partner, we’re here to help. Reach out to NEOREX CRO to learn how we can support your goals with precision, integrity, and scientific excellence.

Let’s Start the Conversation