Ensuring timely and accurate Regulatory submissions can be a daunting task. The volume of processes, systems, and supporting tools needed to plan, track, author, publish, and submit to Health Authorities can be staggering. The process can be more complex when global affiliates require Rest of World (ROW) submissions.
While many pharma companies search for ways to simplify the completion of the seemingly myriad tasks and streamline processes throughout the journey, it can be a heavy lift just to prepare for a confident start. And, if coordination between multiple, related organizations, isn’t fully considered and completed, it poses challenges known to detour—and even derail—timetables.
Please Join us for this informative webinar with our RIM expert, Heather Adinolfi, as she provides you with specific strategies and tactics to: