Solutions
At YATO, we partner with passion to accelerate the delivery of life-changing medicines to patients in need. By embracing the patient perspective, enhancing our impact through operational excellence, and providing integrated solutions and expertise, we support you through every phase of clinical development.
Solutions During Drug Development
Discovery
Early Stage
Early Stage
Portfolio Management & Asset Valuation
Unlock your portfolio’s full potential with optimization strategies that encompass every facet of drug development. Leveraging our integrated expertise in clinical, regulatory, and market access strategy and planning, we empower you to make earlier, faster, and more informed decisions regarding risk and reward, ensuring that each asset has the best opportunity for success.
Early Stage
Early Stage
Early Stage
Early development and innovation
Concluding portfolio management and asset valuation we begin
looking into employing a cohesive strategy that addresses all facets of the development process, we facilitate quicker decision-making while laying a solid foundation for later-stage projects. Our guidance includes biomarker selection, recruitment of healthy volunteers or patients, safety considerations, supplies and logistics, regulatory strategy, and more.
Late Stage
Early Stage
Late Stage
Integrated Clinical Development
Leverage our comprehensive whole-study solutions, crafted to prioritize patient safety, data integrity, regulatory compliance, and scientific rigor. Our integrated strategies not only address these key priorities but also minimize burdens, mitigate risks, and enhance operational efficiency within timelines and budgets, all while keeping patient needs at the forefront of our efforts.
Late Stage
Post Approval
Late Stage
Approval and Access
Collaborate with our team of former regulators and health technology assessment (HTA) professionals who have significantly influenced the current landscape. We apply our extensive expertise to guide you through global regulatory submissions, compliance activities, market access strategies, launch planning, and more, offering advice customized by our localized knowledge and broad therapeutic expertise.
Post Approval
Post Approval
Post Approval
Value Substantiation and Lifecycle Management
Enhance your value narrative and maximize your product’s impact through effective value substantiation and lifecycle management. Our integrated team harnesses real-world evidence (RWE), regulatory insights, and therapeutically focused medical writing to strengthen your value proposition, provide data that meets the expectations of payers and regulators, and foster trust among patients and healthcare providers.
Contact Us
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We love our customers, so feel free to visit during normal business hours.
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