02 / CRO · CLINICAL RESEARCH
Turning innovation into
credible clinical evidence
LIFE LOGICA is preparing CRO support for clinical research, including project management, site coordination, Study Start-up, Site Management, and monitoring. Scope will depend on study type and applicable requirements.
Company formation and service operations are in preparation. These pages describe planned scope; availability and delivery details will be confirmed before launch.
Core Services
Planning for clinical research from design to delivery
The planned scope includes study start-up and site operations, with the requirements confirmed for each study.
Clinical trial project management
Designing a study-specific approach to progress, quality, budget, and risk management.
Site coordination
Reviewing collaboration requirements with hospitals, universities, and clinical partners to plan the study team.
Clinical research consulting
Clarifying research strategy, applicable requirements, and commercialization questions for each study or product.
Study Start-up
Mapping protocol, site selection, contracts, and ethics review steps needed before a study begins.
Site Management
Planning roles and communication with study sites, including enrollment and data-quality responsibilities.
Monitoring
Periodic site visits and protocol-adherence checks, working to safeguard study quality and subject rights.
Partnership model: The planned operating model includes specialist partners for data management and statistical analysis. Partners and scope will be confirmed for each study after the operating structure is established.
Evidence Chain
From study design to commercialization support
STEP
Study design
Planning and operational design of clinical research and trials.
STEP
Hospital & investigator coordination
Coordinating hospitals, universities, and clinical partners.
STEP
Data & evidence
Study operations, data processes, and high-quality evidence generation.
STEP
Development support
Clinical development, regulatory strategy, and commercialization consulting.
Compliance
The value of evidence is built
on compliance
The planned scope would be defined for each project after reviewing the Japanese clinical research rules, GCP, privacy, oversight requirements, and contracted responsibilities that apply to that study type.
Planned approach to GCP and related standards
Before services begin, applicable standards and responsibilities would be reviewed for each study type, then the required procedures and roles defined. This does not represent a current operating GCP system or guarantee compliance.
Privacy protection
Reviewing study-specific requirements for collecting, sharing, and storing personal information, then designing appropriate controls.
Specialized oversight
Identifying the reviews, oversight, and operating procedures required for each study and division of responsibilities.
Quality culture
"Verifiable and commercially viable" is the bar we hold every deliverable to.
Frequently Asked Questions
Clinical research and CRO support
What is included in the planned CRO support?
The planned scope includes clinical research consulting, project management, site coordination, Study Start-up, Site Management, and monitoring. Exact scope depends on the study type and applicable requirements.
Will LIFE LOGICA handle data management and statistics?
The planned operating model includes specialist partners for data management and statistical analysis. Partners and scope will be confirmed for each study after the operating structure is established.
Does GCP apply to every clinical study?
Applicable laws and standards depend on the study type and purpose. Requirements are reviewed for each project before the operating plan is set.
Are these services available now?
Company formation and service operations are in preparation. Launch timing and delivery scope will be confirmed before services begin.
Your innovation deserves
credible evidence
Tell us the purpose of your study and the support you may need. We can discuss the scope currently being planned.