In addition to various traditional evaluation models, we provide comprehensive preclinical drug efficacy pharmacology research, including evaluation models using patient-derived samples, advanced animal imaging analysis, toxic pathology, biomarkers, DMPK analysis, PK/PD modeling, and consulting services.
TAILORED FULL-SERVICE SOLUTIONS
Providing customer-oriented and optimized evaluation services utilizing a patient information integration model
One-stop services for clinical and non clinical support
Quality Assurance System
APEX establishes written operating procedures to ensure consistent, high-quality services for clients and to efficiently conduct tasks related to preclinical studies.
Our Policy
Establishing global regulatory documentation through strategic partnerships with our global clinical trial center and leading international institutions
Global coverage services by implementing the Common Technical Document (CTD) system
Establishing of a quality enhancement system to maintain strict quality control and continuous improvement
Monitoring and improvement of service quality through the validation of each efficacy assessment method
Real-time tracking of progress and sharing of test results through our online project management system
Tailored test analyses through real-time discussions
QA operations under direct oversight of the center director
SOP validation through QA inspections
Conducting tests and documentation according to standardized protocols
Building a collaborative partnerships with clinical and preclinical CROs and advanced medical complexes, etc
Protection of client intellectual property through Confidential Disclosure Agreements (CDA)
Providing security training and securing individual confidentiality agreements from PIs, PMs, researchers, and advisors
Use of a security platform