Comprehensive Solutions. Seamless Execution.
Services
At NEOREX CRO, we provide end-to-end clinical research and licensing services designed to support pharmaceutical and medical device companies at every phase of their development journey. Whether you're launching a first-in-human trial or preparing for product registration, we offer the expertise, infrastructure, and scientific oversight to deliver high-quality results — on time and in full compliance with international standards.
Neorex Cro
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
Neorex Cro
Protocol & Training Services
- Protocol development in collaboration with our scientific board
- Site and investigator training in GCP, study procedures, and compliance
Neorex Cro
Clinical Operations Consultancy
- Tailored consulting for operational planning and study design
- Support for market entry and regional expansion strategies
Neorex Cro
Medical Monitoring & Safety Oversight
- Medical oversight from experienced physicians and specialists
- Pharmacovigilance and adverse event management
- Ongoing safety data review and analysis
Neorex Cro
Study Start-Up Services
- Contract and budget negotiations
- Regulatory document collection and submission
- Site initiation and pre-study visits
Neorex Cro
Feasibility & Site Selection
- Data-driven feasibility assessments
- Strategic site selection
- Collaboration with investigators to optimize trial success
Neorex Cro
Site Relationship Management
- Development and management of a high-performing site network
- Relationship building with investigators and institutions
- Site training and continuous engagement
Neorex Cro
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
Neorex Cro
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
Neorex Cro
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