Advancing medical research through expert clinical trial execution and trusted regulatory guidance.
● About YNNO
About Us
Who We Are
A Clinical Research Center Built on Expertise and Integrity
YNNO Clinical Research Center was founded by two siblings who combined over 21 years of global clinical research operations experience with physician-led expertise in advancing innovative therapies into clinical practice. The center specializes in clinical immunology, allergies, vaccines, and internal medicine, delivering patient-centered research grounded in scientific rigor and accountability.
Supported by advanced digital infrastructure and streamlined processes, YNNO ensures operational excellence, regulatory readiness, and efficient collaboration with sponsors and CRO partners.
Core Values
Key Principles That Define Us
YNNO Clinical Research Center operates on the following key principles:
01
Patient-Centered Care
Every patient receives respectful, empathetic, and individualized attention.
02
Scientific Integrity and Regulatory Excellence
Adhering to the highest standards of ethics, accuracy, and compliance in all research activities.
03
Quality Over Quantity
Emphasizing focused, high-performance study execution rather than high-volume operations.
04
Specialized Expertise
Dedicated to Clinical Immunology, Allergies, Vaccines, and Internal Medicine.
05
Transparent & Direct Collaboration
Sponsors and CRO partners engage directly with leadership, ensuring clear communication and accountability.
06
Integrated Digital & Biomedical Systems
Combining advanced digital systems and biomedical equipment for data integrity, compliance, and reliable study execution.
Our Team
The Experts Behind Clinical Excellence
Meet our team of experts driving operational excellence, regulatory readiness, and meaningful outcomes.
Our Facilities
State-of-the-Art Research Infrastructure
Advanced clinical and digital systems designed for precision, performance, and regulatory-ready execution.
Research Infrastructure (For Patients)
YNNO Clinical Research Center operates within a boutique, quality-driven clinical environment dedicated to clinical immunology, allergies, vaccines, and internal medicine. The facility integrates advanced biomedical technology with focused, patient-centered care to ensure safety, precision, and consistent high-quality study execution.
Digital and Operational Infrastructure (For Sponsors & CRO)
YNNO’s secure digital systems and streamlined workflows support regulatory alignment, data integrity, and operational readiness. Leadership-driven oversight and direct sponsor collaboration enable agile, compliant, and high-performance study execution within a specialized and technology-enabled research setting.
End-to-End Clinical Research Support
Specialized clinical and regulatory services designed to ensure efficient, compliant, and high-quality study execution.
Clinical Trial Site Operations
YNNO Clinical Research Center conducts phase II–IV clinical studies within clinical immunology, allergies, vaccines, and internal medicine. Trials are executed through a boutique, quality-driven model that prioritizes regulatory compliance, patient-centered oversight, and accurate, high-quality data generation.
Leadership-led clinical operations, streamlined workflows, and advanced digital systems ensure efficient study conduct and consistent regulatory alignment. Each study is managed with focused attention, scientific rigor, and operational precision to deliver reliable outcomes for sponsors and CRO partners while maintaining the highest standards of patient safety and care.
Regulatory Consultancy for Sponsors and CROs
YNNO Clinical Research Center provides regulatory consultancy focused exclusively on local regulatory requirements in Mexico, supporting sponsors and CROs without a local presence. This service offers strategic guidance and document preparation support without functioning as a CRO.
Support includes advisory services on Mexican clinical research regulations, preparation of submissions to Ethics and Research Committees and COFEPRIS, guidance on local timelines and processes, regulatory dossier organization, and importation requirements for investigational products, medical devices, and ancillary supplies.
