OUR SERVICES
Advancing Diversity in Clinical Trials (ADVCT)
We understand the importance of inclusive and efficient clinical research.
As a Site Management Organization (SMO), we support your clinical research efforts by providing essential services to a wide range of organizations involved in clinical trials:
We serve:
Contract Research Organizations (CRO)
Pharmaceutical Companies
Biotechnology Companies
Medical Device Companies
Clinical Research Sites
Other institutions conducting clinical trials
How we can help:
Our team of experts offer a comprehensive suite of services designed to streamline your clinical research process and ensure successful study execution.
Principal Investigator Recruitment
Finding the perfect Principal Investigator (PI) is crucial for the success of your clinical trial. At ADVCT, we understand this importance and take the guesswork out of PI recruitment.
Targeted Search: We leverage our extensive network to identify qualified PIs with the specific expertise required for your unique trial.
Matching Credentials: Our team meticulously reviews PI credentials, ensuring they meet your study's protocol and regulatory requirements.
Experience Matters: We prioritize PIs with a proven track record of successful clinical trial leadership.
Patient Recruitment
We manage patient recruitment and retention focusing on achieving enrollment of ethnically diverse populations, women, and elderly patients in clinical trials.
Targeted Outreach: We leverage a variety of methods, including online platforms, patient advocacy groups, and community partnerships, to connect with individuals who meet your study's specific criteria.
Diversity at the Forefront: We prioritize inclusive recruitment practices to ensure your trial reflects a broad patient population, enriching your research data and generalizability.
Streamlined Screening Process: Our team efficiently manages the patient screening process, minimizing administrative burdens and expediting enrollment.
Comprehensive Study Management
At ADVCT, we understand that successful clinical research requires meticulous attention to detail. We offer comprehensive study management services to ensure your trial runs smoothly and adheres to the highest standards.
Trial startup, site initiation, and closeout operations.
Data and regulatory management
Budget and contract management.
Informed consent forms (ICF), recruitment materials, and contracts.
Monitoring and Ensuring Protocol Compliance
Submission for IRB/IEC Approval
Let's Talk
Partner with ADVCT and gain access to a team of experienced professionals dedicated to overseeing every aspect of your clinical trial, from regulatory compliance to data quality.