MCRA has established strategic partnerships with several leading data management companies, each with over 15 years of clinical trials experience. Each company offers proven solutions in electronic data capture (EDC), clinical data management (CDM), and adverse event reporting (AER). Each software platform provides an integrated clinical data management solution that leverages the power of the Internet to accelerate the clinical trial process and helps to ensure rapid database lock and facilitate FDA approval. Additionally, each web-based solution reduces the cost of delivering medical devices to market and transforms the current time-consuming paper based process. At MCRA, we believe that by providing our clients with data management options we can customize the data management program to suit the exact needs of each of our clients.
|Streamlined data collection and data cleaning|
|Electronic case report forms with a complete audit trail of all data entered and modified|
|Online patient enrollment and randomization|
|Integrated Central Coding solution|
|Online automated and manual query creation, resolution and tracking|
|Complete study monitoring tools|
|Integrated online protocol and eCRF completion guidelines|