July 10-11, 2017 Philadelphia, PA
Regulatory submissions are critical in clinical research and it’s important that regulatory professionals properly manage submissions. The regulatory submissions process can quickly become challenging when multiple team members are involved, and it is essential to ensure the quality and consistency of each document included in a submission. Doing so from the earliest stages of a product’s development benefits your organization.
The eRegulatory Submissions Summit will cover electronic submission processes and protocols for constructing strategies for IDMP, RIM, global and regulatory submissions. This summit will also address regulatory information management experiences and the proposed new standards for the identification of medicinal products. Come hear the latest guidelines on eCTD and how to successfully submit an electronic submission.
