Phase I Clinical Trial Support
Facilitating early-stage clinical studies, particularly Phase I Oncology Trials, to evaluate the safety and tolerability of investigational drugs.
Facilitating early-stage clinical studies, particularly Phase I Oncology Trials, to evaluate the safety and tolerability of investigational drugs.
Clinical trial protocol design and consultation.
Recruitment and management of study subjects.
Safety monitoring and reporting.
Data analysis and regulatory reporting.
Ensures smooth transition from preclinical to clinical phase.
Minimizes risks by providing expert trial design.
Provides reliable, regulatory-compliant results.