Clinical Trial Site Development by Global MedTrial LLP
Transforming Institutions into High-Performing Clinical Trial Sites
At Global MedTrial LLP, we are committed to revolutionizing the clinical research ecosystem by developing quality-driven, globally competitive clinical trial sites. Through our specialized business models, we collaborate with medical institutions, hospitals, and clinics to build and operate efficient, GCP-compliant, and sponsor-ready clinical trial facilities.
Whether you’re launching your research capabilities or aiming to scale your operations, our clinical site development solutions ensure strategic growth, regulatory compliance, and global competitiveness.
Exclusive Site Model
Complete Clinical Research Operations for Naive Sites
This model is ideal for institutions with no prior clinical research experience but with the potential to become high-performing trial sites. Under an exclusive agreement, Global MedTrial LLP works as an internal clinical trial department, not as an external vendor, to design, develop, and manage all aspects of clinical trial operations.
We build an in-house clinical research infrastructure from the ground up and embed a dedicated team to ensure seamless operations and regulatory readiness.
Key Features
- Ideal for greenfield research site development
- Stepwise implementation of clinical trial readiness
- Holistic training and compliance programs
Services Offered
- Facility layout planning and optimization for research use
- Infrastructure procurement and installation (e.g., temperature-controlled storage, secure document rooms)
- End-to-end formation of a Clinical Trial Department
- Hiring and deployment of site staff (CRC, CTA, Pharmacist, Data Entry Operator)
- Development and implementation of institution-specific SOPs
- Training programs on GCP, ICH, ICMR, NDCT Rules, and local regulations
- Regular workshops on regulatory and operational updates
- Site-specific business development and study onboarding
- Clinical trial operations management (site feasibility to close-out)
- Sponsor and CRO coordination for smooth site conduct
- Study start-up support including contracts and budget negotiation
- Liaison with Institutional Ethics Committee (IEC)
- Safety reporting procedures and SAE management
- Comprehensive archiving and regulatory documentation systems
- Performance monitoring and continuous quality improvement plans
Affiliated Site Model
Complete Clinical Research Operations for Naive Sites
Our Affiliated Site Model is designed for hospitals, clinics, and institutions already conducting clinical research and looking to enhance performance, scale operations, and attract more studies. Global MedTrial LLP offers modular and customizable support tailored to your operational gaps and growth targets.
This model enhances your site’s visibility among sponsors while streamlining operations for increased quality and compliance.
Key Features
- Flexible, need-based engagement
- On-demand operational and regulatory support
- CRCs can be deployed study-wise based on sponsor requirements
Services Offered
- Infrastructure planning to expand trial capacity (labs, archives, IP storage)
- Consultation on clinical research staffing and HR support
- GCP training and role-specific workshops (PI, CRC, Pharmacist)
- CRC deployment (temporary or long-term based on sponsor/site need)
- SOP customization and optimization for trial efficiency
- Business development support to increase trial opportunities
- Documentation assistance for trial master file and source documents
- Study start-up consulting (site selection, regulatory approval process)
- Protocol feasibility analysis and implementation planning
- Operational gap analysis and solution implementation
- IEC interaction and compliance support
Clinical Trial Foundation Model
Structured Program to Establish Clinical Research Units
The Clinical Trial Foundation Model is crafted for institutions aiming to enter the clinical research domain. Our foundation program provides a step-by-step roadmap to build infrastructure, train staff, and establish regulatory-compliant systems that are essential for initiating and sustaining clinical trials.
This model lays a robust foundation to convert your hospital/clinic into a sponsor-ready research site.
Key Features
- Ideal for greenfield research site development
- Stepwise implementation of clinical trial readiness
- Holistic training and compliance programs
Services Offered
- Site infrastructure assessment and customized development plan
- Facility and spacing strategy for research operations
- Assistance in forming a dedicated Clinical Trials Department
- Identification and training of site leadership and research staff
- Preparation of SOPs aligned with global standards and Indian regulatory norms
- GCP and regulatory training (NDCT 2019, ICH-E6)
- Hands-on operational training for CRCs and investigators
- Support in setting up the Institutional Ethics Committee (IEC)
- Documentation control systems and archiving SOPs
- Safety reporting training and SAE handling practices
- Mock site readiness inspection to ensure audit compliance
- Sponsor-readiness evaluation and quality control
Clinical Trial Support Model
Operational, Quality, and Compliance Support for Active Sites
For sites already conducting trials, our Support Model offers ongoing operational optimization, regulatory training, and audit readiness. This model is ideal for institutions aiming to elevate their quality standards to international benchmarks, manage audits, or attract global sponsors.
Whether you’re preparing for a sponsor inspection or strengthening internal SOPs, our clinical trial support solutions help you stay competitive and compliant.
Key Features
- Scalable support services for growing sites
- Designed to enhance operational efficiency and compliance
- Helps improve sponsor satisfaction and audit outcomes
Services Offered
- Clinical trial staffing consultation and interim resource deployment
- GCP and protocol-specific training for site staff
- Quality Assurance: Internal quality audits, CAPA planning
- System audits (data handling, document control, IP management)
- Vendor audits and regulatory inspection readiness
- Ethics Committee training on GCP and compliance standards
- Safety and SAE management training
- Development of trial-specific documentation processes
- SOP review and refinement
- Periodic site performance reviews with gap analysis
Why Partner with Global MedTrial LLP?
- Experienced Clinical Development Experts with a track record of transforming research sites
- Proven Frameworks for operational excellence, compliance, and sponsor engagement
- Dedicated Teams for Business Development, Operations, and Regulatory Affairs
- On-Site Presence ensuring seamless integration with your institution
- Training-Oriented Approach to ensure long-term sustainability
- Sponsor and CRO Network to accelerate study onboarding
Let’s Build the Future of Clinical Research Together
Ready to unlock your institution’s clinical research potential?
Contact Global MedTrial LLP today to explore how we can help you launch or grow your clinical trial site with the right expertise, infrastructure, and strategic support.