Clinical & Regulatory Support Services
Clinical development and regulatory oversight demand accuracy, transparency, and strict adherence to international guidelines. Ethiqx provides comprehensive clinical and regulatory support services to ensure smooth trial execution, compliant documentation, and efficient approvals.
Clinical Trial Support
End-to-end management of clinical studies, from protocol development to site monitoring and trial oversight.
Regulatory Affairs
Preparation, review, and submission of regulatory dossiers to global health authorities.
Data Management & Biostatistics
Collection, analysis, and interpretation of trial data with precision and reliability.
Safety & Vigilance
Pharmacovigilance and safety monitoring services that protect patients and maintain compliance.
Technology & Automation
Integration of digital tools to improve efficiency, accuracy, and data quality.
Key Features
- Global trial compliance with FDA, EMA, ICH, and WHO standards.
- Experienced teams in clinical documentation and regulatory filings.
- Technology-enabled processes for efficiency and accuracy.
- Proven track record in managing multi-country trial submissions.