Authoring Efficiencies and Cross-functional Strategies: Clinical Study Report and Beyond

This Expert Insights webinar presentation from MMS Holdings will focus on providing insights into pharmaceutical industry trends and strategies for targeted, efficient Clinical Study Report (CSR) authorship. Medical writing experts will discuss recent technological advancements, writing efficiencies, and a top-to-bottom integration approach across key stakeholders to produce high-quality CSRs that are FDA/EMA submission- and clinical trial disclosure-ready. Best practices for authoring strategies will span across medical writing portfolios and document types.
Attendees will learn:
-Approaches in combining technology, strategic authoring, and cross-functional collaboration to maximize document quality and compliance
-How to reduce overall effort and time expenditure
-Strategies for proactively addressing regulatory agency requirements in CSR authorship
-Considerations for key stakeholders including members of the document publishing team
-How to remain flexible in the current regulatory landscape
Presenters:
Michelle Reed, PhD, Medical Writer
Jessica Murdock, PhD, Senior Medical Writer

[@sekharPharma]

Thanks a lot

[@yumingzhao5577]

Excellent presentation