David Morris Email & Phone Number

Participated in meetings with regulatory agencies in the United States (eg, CDER, CBER, and CVM), Canada, and Europe (eg, United Kingdom, Netherlands, and Germany). Provided statistical representation for sponsors at FDA public advisory committee meetings.Assisted in clinical trial design and written statistical analysis plans for clinical trials in psychiatry, analgesia, iron deficiency anemia, antibiotics, erectile dysfunction, arousal disorder, tropical diseases, and animal products.Written clinical overview documents (ISE, ISS, Module 2.7, and/or Module 2.5) in analgesia, epilepsy, iron deficiency anemia, inflammatory bowel disease, testosterone replacement therapy, gene therapy, and malaria. Written briefing documents for FDA meetings (eg, end of Phase 2 and pre-NDA) and FDA public advisory committee meetings.Co-author of published articles on clinical trial results in iron deficiency anemia, analgesia, bipolar disease, schizophrenia, and insomnia.

Listed skills include Clinical Trials, Cro, Regulatory Submissions, Oncology, and 15 others.