Рет қаралды 757
This webinar covers the pathways for regulatory review and approval for cell and gene therapies in the United States and Europe. The speakers discuss the regulatory frameworks, sponsor interactions with Health Authorities, accelerated regulatory pathways, as well as submission content for clinical trials in these two major markets.
Speakers:
Michael Mendicino, Ph.D., President, Chief Consultant & Advisor, Hybrid Concepts International
Emmanuelle Sabbah-Petrover, Ph.D., Regulatory Science, Cell & Gene Therapeutic Products, Voisin Consulting Life Sciences