Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
The COVID-19 pandemic has upended the working norms of every sector, but perhaps no industry has been challenged quite so much as those businesses in life sciences. The importance of speed, and expediting the drug documentation approval process, took on a whole new meaning during the pandemic.
Yseop’s new whitepaper looks at how recent global events have served as a catalyst for change for pharmaceutical companies. It has fundamentally altered the drug application approval process and introduced the rise of new technologies, like AI and NLG. Firms have had to pivot to new strategies like:
In this whitepaper, we look at the rise of new strategies that help firms get drugs to market safely, challenges this technology faces from the people who use it, and the opportunity to rewrite processes for the future.