At Curavit, we offer feasibility and protocol development services that blend scientific expertise with operational practicality, always staying up to date with FDA draft guidance. Our cross-functional team works collaboratively to ensure your study design is both effective and executable within the regulatory and healthcare landscape.

Curavit will streamline your regulatory path with proactive strategies that minimize compliance risks and accelerate approvals. Our experts guide you through every step to maximize your treatment’s market potential.

Curavit accelerates trial start-up by identifying top-performing sites. We have established partnerships with the leading national site networks, matching the right patients and coordinating teams around your protocol. Our site strategies focus on diversity, performance, and delivery from day one.

Curavit removes barriers to access through personalized outreach, education, and diversity tracking- ensuring inclusive recruitment and better retention for more representative trial outcomes. We embed diversity principles into clinical program development, regulatory strategy, operational execution, and tailored Diversity Action Plan.

Curavit utilizes a broad range of AI-powered digital tools which enables us to manage the entire enrollment journey, starting with screening and consent, and ending with enrollment. Partnering with advocacy groups and offering concierge services, we support diverse participation and seamless site execution.

Curavit manages the full clinical supply chain and logistics- compliance, documentation, and delivery- through a nationwide depot network to ensure fast, secure, and compliant distribution of study materials.

Curavit’s Virtual Clinical Site enables full remote monitoring, ensuring patient safety, protocol adherence, and retention.

Curavit coordinates external national lab services and home-based healthcare professionals, then integrates results directly into our Virtual Clinical Site.

Curavit’s teams provide real-time monitoring using digital consent, telehealth, and remote data capture to safeguard patient safety and protocol compliance throughout the trial.

Curavit delivers high-quality clinical data from start to submission, offering EDC design, data cleaning, validation, and analytics tailored to your study—supporting confident, timely decisions. We leverage Real World Evidence (RWE) to provide valuable insights, demonstrate cost-effectiveness, and make informed decisions regarding the adoption, pricing, and reimbursement of new therapies and devices.