Our Expertise
AMS combines decades of experience with modern clinical strategies to help optimize the entire lifecycle of your product. Our highly skilled team ensures proper planning, conduct, data quality, and patient safety while building strong relationships between the sponsor and site investigator. AMS combines an innovative, transparent and collaborative work style with extensive experience in early and late-phase studies, as well as non-interventional studies.
Clinical Monitoring & Site Management
AMS provides comprehensive clinical trial monitoring and site management services from trial start up to close-out in sites all over the world. Our global team provides consistent and high-quality standards across all programs by following ICH-GCP and all applicable regulatory guidelines.
AMS’s Clinical Research Associates (CRAs) have extensive clinical research and therapeutic experience, with a strong focus on site relationships. Our CRAs across Europe and our global CRA team operate with specific processes in early development clinical trials or late stage projects, respectively.
AMS operates a fully validated and easy-to-use EDC system, as well as a BYOD electronic patient-reported outcome (ePRO) solution. These provide new opportunities in collecting data directly from patients.
Project Management
The PM-concept of any project is an essential factor of success. AMS’s Standing Out From the Crowd project management concept helps ensure you stay on budget, within project timelines, and that data quality is maintained.
Our AMS project managers work closely with you and your team to coordinate all project related tasks, provide a robust plan for the project progress and associated timelines, and implement technological solutions such as EDC-derived management reports, collaboration platforms, and document management systems.
Investigator and Site Feasibility & Selection
Conducting investigator and site feasibility is one of the most crucial first steps in clinical trial start-up. We know that in the clinical industry sector, patient recruitment cycle times are getting longer, and in most programs, only 1/3 of investigators are your top enrollers.
The AMS clinical team will steer you in the right direction by ensuring we minimize all of these challenges by ensuring you are at the right site with the right investigator suited for your clinical trial design and indication.
We include the following:
Study and Site Planning
Investigator and Site Feasibility
Site Selection
Budgets & Contracts
We specialize in a variety of services and solutions.
