ClinPlus

ClinPlus’ self-developed big-data modeling system leverages performance data from historical projects to generate site selection, site initiation, patient recruitment, risk, quality, data, patient & investigator cost and other models, delivering precise execution strategies for clinical trials.

To date, ClinPlus modeling data has been validated by over 400 SSU projects and 600+ patient recruitment projects. The matching rates against project plans reach 97.89% and 94.38% respectively. It cuts the strategy development cycle for clinical trial execution from months to just one week.

ClinPlus SSU team covers key regions nationwide, with in-depth knowledge of site workflows. We develop contingency plans to proactively mitigate potential obstacles and risks during site initiation.

After the initiation plan is finalized, ClinPlus SSU Services leverages our innovative site initiation platform to deliver in-depth interpretation of site requirements and clinical trial protocol analysis. The system enables one-click generation of multi-site essential documents, eliminating manual documentation errors and reducing time costs.

ClinPlus delivers customized, professional, flexible and sustainable FSP services for clients.

Dual internal & external candidate sourcing channels; comprehensive training system; full-lifecycle workforce management by dedicated HR teams to boost productivity; diverse career development opportunities for staff.

Backed by a decade of professional experience focusing on SMO services, ClinPlus has established stable long-term FSP partnerships with numerous renowned research sites and sponsors, with some relationships spanning more than 10 years.

ClinPlus quality control team is deployed in core cities nationwide, professionally delivering research site audits, trial document audits, CAPA follow-up until closure, consultation and training services. We ensure all clinical trial procedures comply with GCP, clinical trial protocols, relevant SOPs and applicable laws & regulations.

We supervise project execution, identify and rectify issues in a timely manner, protect the rights and interests of trial subjects, guarantee scientific, authentic and reliable clinical trial data, and ensure standardized operations.