At the time of regulatory submissions, one of the most resource intensive and complex areas is getting the integrated summary... Read More
Categories: Case Study
For an emerging biotech, budgets and resources are typically constrained and it requires an agile data partner to address the... Read More
Categories: Case Study
This US based biopharma company required an electronic submission package for over 13 studies to be submitted to the US FDA. ... Read More
Categories: Case Study
With the ever-increasing number of clinical trials (the gold standard in new therapy evaluation) including those relating to ... Read More
Categories: Covid 19