While on-site monitoring is one of the biggest cost drivers of clinical trial operations, Remote Source Document Verification (rSDV) offers.
Oversight is YOUR responsibility no matter what you outsource and to which vendors you work with. You are accountable fully in the eyes of healthcare regulators.
With the inclusion of centralized monitoring in risk based monitoring (RBM) approach; the Central Monitor is emerging as a key and important role.
If you are part of Regulatory - Labeling team in your company, you should not miss this Webinar. As you are constantly working to coordinate a more robust end-to-end.
Sponsor’s performance of investigational site risk assessment is essential for effective planning and implementation of clinical trial project.
“To Outsource or Not to Outsource”, the question that many of the companies may be asking. The webinar aims to compare and contrast the advantages & disadvantages.
Let's talk about how MakroCare can help you