Eliminate manual process
Our MLM-Lite solution will help automate the process of manually identifying the relevant files that need to be downloaded from the EMA site
According to Good Pharmacovigilance Practices (GVP) Module VI, marketing-authorization holders (MAH) are required to monitor medical literature and to report individual cases of suspected adverse reactions for medicines for which they hold a marketing authorization in the EEA
M-Lite Solution can help eliminate the manual process. Relevant files will be available in R2/R3 ICSR format
Design and deploy additional filters for ICSR Files, based on your requirements.
Enable realtime reports for complex data inline to desired report.
Lack of Artificial Intelligence for ICSR files analysis and reporting.
Various view of reports, automation based on data value.
MLM lite is a fully automated solution to ensure quick turnaround and timely delivery.
MLM lite ensures 100% accuracy in data analysis, tabulation and formated reporting.
MLM lite can be integrated with any existing system or solution with minimum configuration.
MLM Lite has proven track with various pharma companies with 5 Star rating.
MLM LIte is powered by latest and secure technology like coud and bigdata.
With the Help of MLM lite, it is very easy to automate literature data monitoring.
MLM lite is a Regulatory ready solution, so huge time and cost save for pharma companies.
MLM lite is proven tool to process your medical literature data from EMA database and provides interface to pull required data in desired format.
In General we take 4 Weeks time to study and signoff your business requirement.
Yes, we understand your business needs and regulatory requirements. We can customize this solution based on your requirement.
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Olcay have been proven partner for all our pharma needs.
Olcay is our technology partner for regulatory reports.
