For Sponsors

We pride ourselves on the exceptional involvement of our Principal Investigators (PIs) in every study, from feasibility assessments and investigator training to the consenting process for each subject. Patient safety is our top priority, with all staff members maintaining up-to-date GCP certifications and specialized training. Our rigorous procedures include meticulous drug tracking and secure management by the PIs and Clinical Research Coordinators (CRCs), ensuring the integrity of our studies. Additionally, our senior CRCs conduct thorough data validation, ensuring all study information is accurately entered and cross-checked in the Electronic Data Capture (EDC) system.

ICR has a proven track record of successfully executing high-enrollment vaccine studies in partnership with leading pharmaceutical companies like Moderna and Pfizer. Beyond vaccines, our expertise extends to Women’s Health research and investigations into conditions such as Migraines, COPD, Asthma, and other medical areas. To further enhance study reliability, we employ advanced VCT biometric scanning technology to prevent dual enrollment, safeguarding the accuracy and integrity of our data.

Committed to advancing medical knowledge and contributing to a healthier future, we adhere to ICH, GCP, and all regulatory guidelines. Our unwavering focus on patient safety, data accuracy, and operational excellence makes Ideal Clinical Research the trusted partner for your clinical trials. Let us work together to bring groundbreaking medical solutions to life.