Top 20 Pharma selected MakroCare for Centralized Monitoring (CenMon)
MakroCare was approached by a top 20 pharma company to support their centralized monitoring projects. MakroCare, the leader in Centralized Monitoring, with its deep implementation experience helped the client formalize complete process of centralized monitoring and in addition provided technology (ClinMetanoia) as well for generation of the relevant metrics, reports and dashboards.
- Newark, NJ (1888PressRelease) January 07, 2016 - As complexities of clinical trials, have been increasing significantly in last few years; it is becoming challenging for life science companies to manage and monitors their projects, programs to ensure right conduct and obtain desired quality and integrity of the data which is appropriate for regulatory submission within planned timelines and budget.
MakroCare's Centralized Monitoring approach - CenMon offers a smarter, reliable and cost-efficient way to monitor various aspects like RISKS, CLINICAL, SAFETY, QUALITY and also supports OVERSIGHT of their trial, program or project. By aligning right customized processes, robust technology and trained resources, CenMon helps sponsor to take real control of their projects, vendors/CRO and cost.
During the implementation process, MakroCare supported the client starting from risk assessment and identification of the right KRIs as well as KPIs all the way to mitigation and monitoring. ClinMetanoia was used to generate the reports with suggested thresholds and triggers for easy, proactive identification of risk/issue(s). MakroCare also provided trained central monitors to make the overall process cost effective and efficient. MakroCare's CenMon advisory team assisted client with relevant "hand-holding" and provided support for change management as this process is new for the company and it's internal teams. As the industry is actively embarking on the paradigm shift of RBM & Centralized Monitoring, our Centralized Monitoring Service (CenMon) has been supporting clients by aligning right customized processes, robust technology and trained resources, to take control of their early, late phase trials, programs to improve overall quality and create cost efficiencies.
For more details : http://bit.ly/1Peym92
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