Holtz BioPharma Consulting provides services to pharmaceutical developers and manufacturers of biologics to bring products from bench to approval. We facilitate the concurrent development of clinical, manufacturing and regulatory strategies from the earliest point of discovery and development to commercial launch.
Our team has successfully developed regulatory strategies for the clinical delivery of new patient specific medicines, new biologics and "follow-on" biologics. We have also designed ,constructed and operated c GMP compliant biologics manufacturing facilities.
Our consultants are committed to the "business of science" and are dedicated to the completion of projects to a successful commercial endpoint.