AUTOMATING CLINICAL TRIALS The pandemic forced a giant leap in innovation around clinical trials, demonstrating how intelligent automation technologies such as RPA, AI and natural language processing could be used to expedite trial processes and speed up time to market.
DOCUMENT PROCESSING AND STORAGE As a highly regulated industry, life sciences organisations must process and store large volumes of documentation to remain compliant. Intelligent Document Processing and Optical Character Recognition enables structured and unstructured data to be extracted and processed from regulatory documents for easy retrieval and analysis.
ADVERSE EVENT REPORTS Large pharma companies receive hundreds of thousands of Adverse Event Reports every year. Process these reports automatically with RPA to reduce the administrative burden, scaling down costs while enabling increased focus on areas of concern.
BACK OFFICE FUNCTION Automating repetitive tasks in finance, procurement, HR and other back-office teams can make a significant difference to the overall efficiency and reduce the amount of time research professionals need to spend on administration.
REGULATORY REPORTING Regulatory reporting requires standard data to be gathered and collated, and to follow fixed review and submission processes. These can all easily be automated to reduce the administrative burden while maintaining compliance.