Amicis Research Center offers a comprehensive range of services to support clinical trial and site management. We provide a one-stop-shop for our clients, including the following services: study procurement, physician recruitment, patient enrolllment, business development, contract negotiations, site specific clinical research systems, regulatory submissions, training and education.

Therapeutic Areas

We have experience conducting clinical trials across many therapeutic areas, including family practice, internal medicine, nephrology, neurology, pulmonology, rheumatology, infectious disease, OB/GYN, ophthalmology, psychiatry, cardiology, dermatology and others.

Site Selection and Management

We work with you to identify and select clinical trial sites that are best suited to your study. Our team also manages site initiation, ongoing monitoring, and quality assurance to ensure that your study runs efficiently and effectively.

Regulatory Affairs

We have a deep understanding of local and global regulations, and we work with you to navigate the complex regulatory landscape. Our team provides guidance on regulatory submissions, compliance requirements, and audit/inspection preparation.

Data Management

We offer comprehensive data management services, including data capture, cleaning, and analysis. We use cutting-edge tools and techniques to ensure data quality and integrity, and we provide secure storage and backup of your data.

Study Types

We offer a range of study types, including Phase I-IV trials, post-marketing studies, and real-world evidence studies. Our team has experience managing all types of clinical trials, and we work with you to ensure that your study meets its objectives.

Technology and Innovation

We use innovative technologies and approaches to enhance the quality and efficiency of our projects. We use GoTo Coordinator, adaptive trial design, and other cutting-edge tools to help you achieve your clinical trial objectives.