At Cyntax Health Projects Pvt. Ltd., we are committed to advancing healthcare through high- quality clinical research and trials. As a leading Contract Research Organization (CRO), we provide comprehensive solutions for pharmaceutical, biotechnology, and medical device industries, ensuring innovation, compliance, and excellence in every study we conduct.
Our Clinical Research Services
Clinical Trial Management
- End-to-end management of Phase I-IV clinical trials
- Protocol development, site selection, and patient recruitment
- Regulatory submissions and compliance with international standards (ICH-GCP, FDA, EMA)
Regulatory & Compliance Services
- Ethical approval and IRB (Institutional Review Board) coordination
- Preparation and submission of regulatory dossiers
- Post-market surveillance and pharmacovigilance
Biostatistics & Data Management
- Advanced data collection, monitoring, and analysis
- Real-time reporting with cutting-edge software solutions
- Secure and compliant data handling
Site Monitoring & Investigator Support
- Clinical site selection, training, and management
- Patient recruitment and retention strategies
- Continuous site monitoring for quality assurance
Pharmacovigilance & Safety Monitoring
- Adverse event reporting and risk management
- Drug safety assessments and signal detection
- Compliance with global safety regulations
Our Areas of Expertise
- Cardiovascular & Metabolic Disease Trials
- Oncology & Immuno-Oncology Trials
- Infectious Disease Trials
- Rare Diseases & Orphan Drug Research
- Neuroscience