Practical Guidance for Successful Global Regulatory Submissions: Understanding FDA and PMDA Data Standards Requirements, Upcoming Webinar Hosted by Xtalks

In this free webinar, gain insights into the constantly evolving data standards requirements for regulatory submissions. The US Food and Drug Administration (FDA) and Japan's Pharmaceuticals and Medical Devices Agency (PMDA) delineate these requirements through binding guidance documents,...
Source: PRWeb: Medical Pharmaceuticals - Category: Pharmaceuticals Source Type: news