SRD ClinMax is a global Clinical Research Organization (CRO) providing clinical trial management, regulatory consulting, and data management services for pharmaceutical and medical device companies in the USA, Japan, and China.

Our expert team manages end-to-end clinical trial operations, including protocol design, site selection, patient recruitment, regulatory submissions, and trial data analysis, ensuring compliance with FDA, PMDA, and NMPA standards.

With offices in San Francisco, Tokyo, and Beijing, SRD ClinMax offers cross-border clinical trial expertise and regulatory intelligence across North America and Asia, helping clients accelerate drug development and market approvals.

Yes, our regulatory affairs specialists assist in preparing clinical documentation, navigating FDA/PMDA/NMPA submissions, and managing post-approval compliance for both pharmaceuticals and medical devices.

We follow ICH-GCP (Good Clinical Practice) standards and implement strict data integrity protocols throughout every stage of clinical trial management, ensuring reliable, compliant, and auditable study results.

Our unique foundation as a Japanese-Chinese joint venture CRO allows us to combine Asian market expertise with Western regulatory knowledge, offering truly global clinical trial solutions for pharmaceutical innovation.

Absolutely. Our Site Management Organization (SMO) supports investigator site selection, patient recruitment and retention, and clinical site monitoring to ensure each study meets its enrollment goals and timelines.

We manage Phase I–IV clinical trials, post-marketing surveillance, and medical device evaluations across therapeutic areas such as oncology, cardiology, neurology, and rare diseases.

Sponsors can reach out through our contact form or email kevinlee@srdclinmax.com to discuss clinical trial feasibility, regulatory pathways, or contract research collaboration opportunities.

SRD ClinMax operates from San Francisco (USA), Tokyo (Japan), and Beijing (China), providing local regulatory support and global clinical trial coordination for clients across North America and Asia.