We advance healthcare through evidence-based research that drives innovation and improves patient outcomes.
At Evidenica, we provide comprehensive, start-to-finish clinical research solutions tailored to the unique needs of sponsors, investigators, and healthcare innovators. Our end-to-end clinical research management ensures your study is expertly guided through every phase—efficiently, ethically, and in full regulatory compliance.
Study Planning & Protocol Development
We help you build a strong foundation. Our experts assist in study design, protocol writing, site feasibility, and regulatory documentation—ensuring your trial is strategically positioned for approval and success.
Regulatory Submissions & IRB Support
Our team streamlines the complex process of submitting your study to ethics boards and regulatory agencies, including FDA or EMA filings, amendments, and ongoing reporting.
Site Management & Patient Recruitment
We identify, activate, and manage high-performing clinical trial sites. Our recruitment strategies are patient-centric, ensuring diverse enrollment, rapid onboarding, and high retention rates.
Monitoring & Data Collection
Our experienced CRAs (Clinical Research Associates) ensure on-site and remote monitoring, data accuracy, GCP compliance, and risk-based quality assurance throughout your study.
