Medical Affairs

At Medivant Pharma, we offer comprehensive medical affairs services to ensure the integrity and quality of your clinical trials. Our services include:

1. Patient Recruitment & Site Management
   
   • Proven strategies for patient recruitment across diverse demographics.
   • Global network of high-performing clinical sites to optimize trial efficiency.
2. Medical Monitoring
   
   • Full-service medical monitoring to ensure trial integrity and safety.
3. Quality Assurance & Compliance
   • Rigorous quality assurance processes aligned with GCP and global regulatory standards.
   • Audit-ready services ensuring compliance and high-quality trial outcomes.
4. Pharmacovigilance & Safety Monitoring
   • Comprehensive drug safety monitoring, from adverse event reporting to risk management.
   • Expertise in post-marketing surveillance and safety data collection.
5. Project Management & Strategic Consulting
   
   • End-to-end project management to deliver trials on time and within budget.
   • Strategic consulting to align clinical development with commercial objectives.
6. Global Reach & Market Expansion
   • Extensive experience in LATAM, US, and EU markets for clinical trials.
   • Expertise in navigating regional regulatory landscapes for faster approvals.