Improves the efficiency of CRAs, as they concentrate on the sites that need help and allow competent sites to proceed without unnecessary interference.
Time is an important element of any research activity. New and emerging challenges place an increasing pressure on decision makers in the pharmaceutical industry to search for an optimal/near-optimal resource utilization plan that minimizes research time while maximizing its quality.
Your Data is our Priority. The collection of high quality clinical data is our priority as we understand that high quality clinical data is the only difference between success and failure of a clinical trial. We offer data management service
ACT provides complete support and maintenance services for all projects, thereby enable our clients to focus on their core business as well as helping them leverage Research & Development rather than just manage it. Technical documentation: We provide complete documentation for all the
Our team of expert auditors ensure that the serviced client business is in compliance with current regulations. We perform a detailed assessment of the processes in place and will identify areas of improvement and recommend suggestions. We provide assistance inRead more
The three main stakeholders in our medical writing department are medical writers, regulatory experts and scientific affairs. Our team has expertise is various writing styles and formats always ensuring compliance with ICH-GCP with both client templates and/or our templates WeRead more