SERVICES

Associated Medical Clinical Science Services is an full service clinical research organization for the development of drugs, biologics and medical devices in order to promote therapy and to prevent diseases. It is our mission to develop, register and market new drugs in the shortest time possible and under strict adherence to ICH GCP guidelines.

We value the individuality of our sponsors, and understand that one sponsor will require something entirely different to the next. We aim to provide you with a service that matches your exact requirements throughout the entire lifecycle of your clinical study.

AMCSS can provide following services:

• Project Management
• Ethics committee submission and management
• Ongoing medical review of all CRFs
• Full study set-up, including: investigator identification, selection and recruitment
• Investigator grant negotiation and administration
• Regulatory Document Management
• Quality Assurance (Protocol / CRF Review, Trial Master File Audit, Investigator Site Audit, Clinical Study Report Audit)
• Feasibility
• Investigator Meeting Preparation
• Site Initiation
• Study site management
• Clinical Monitoring
• Patient Recruitment Support
• Trial Master File Management