Your dedicated partner in delivering personalized and efficient solutions for all your clinical research needs. Our comprehensive range of services to support Phase I to IV Clinical Trials include the following :
From a project’s inception until its successful completion, we carefully coordinate and execute each step.
Site Management
Pre-identified partner sites trained to work on StriderDCT’s technology platform and SOPs efficiently.
Regulatory Affairs
From submissions to approvals in compliance with local/international regulations. Extensive network of consultants and advisors for niche requirements.
Clinical Monitoring
From source data verification to risk-based monitoring to ensure data accuracy and participant safety.
Data Management
With advanced systems, we collect, clean, and analyze data meticulously.
Biostatistics
From trial design to analysis, our biostatisticians provide unparalleled statistical support.
Medical Writing
Creating essential documents – protocols, clinical study reports, and other regulatory documents.
Pharmacovigilance and Drug Safety
The pharmacovigilance team meticulously monitors, evaluates, and reports adverse events, upholding safety standards throughout the trial.
Quality Assurance
We conduct audits, inspections, and assessments, ensuring every aspect meets the highest standards.
Vendor Management
Utilize our strategic partners worldwide or work with your preferred collaborators.
