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Delivering a complex ISS/ISE submission

At the time of regulatory submissions, one of the most resource intensive and complex areas is getting the integrated summary... Read More

Supporting an emerging biotech with end-to-end data services for an oncology product

For an emerging biotech, budgets and resources are typically constrained and it requires an agile data partner to address the... Read More

Case Study - Expediting complex regulatory submissions with MetaVate

This US based biopharma company required an electronic submission package for over 13 studies to be submitted to the US FDA. ... Read More

Statistical methods for handling missing data in clinical trials during COVID-19

With the ever-increasing number of clinical trials (the gold standard in new therapy evaluation) including those relating to ... Read More