This series of training courses is co-organized by MinYue-Pharos Consulting, LLC and DrugTimes, presented by American experts with decades of experience in US and global pharmaceuticals, medical devices, and IVD registrations. The training series includes: webinar, on-site lectures, on-site product development guidance, and consulting on China/US/Global clinical and registration strategies and implementation. The training will be conducted in the form of online video, after which American experts will come to China to conduct face-to-face training and answer questions.
For webinar, FDA regulations training course (drugs, biological products):
60 hours of study. Through study, students and friends will have a systematic and in-depth understanding of the latest FDA regulations, and can immediately apply in pharmaceutical research and development. This course is suitable for R&D professionals in pharmaceutical R&D companies, biotechnology companies, clinical experts, lecturers or students of university regulatory affairs, and professionals engaged in registration, clinical supervision, quality system creation and management.