Works with a competent financial team with extensive experience in Contracts & Budget Review, and managing financial concerns of the project.
Boasts of extensive experience on EC/Regulatory Submissions. Partner Site has PHREB Level 3 Accreditation IRB which facilitates EC review and approval in an efficient manner, and may accept expedited review within the IRB guidelines.
Access to professionals who are proficient in developing protocol and trial related forms.
Access to a network of skilled and knowledgeable Clinical Research Associates who can provide support on the monitoring activities of the clinical trials.
Recruitment and Retention System, Compliance and Data Quality Control, Subject Safety Monitoring, Site Staff, Project Lead, and Others.
Access to a network of Statisticians with wide experience on Clinical Trials and other types of researches.
Ensures that feasibility/qualification data are provided at the fastest period to CROs/Sponsors.