Amanda M. Radspinner, Ph.D., RAC has over twelve years experience in the pharmaceutical industry both in the US and abroad Europe. This includes over ten years experience with postapproval regulatory CMC submissions, as well as extensive experience in developing and preparing CMC sections for investigational drug substances and drug products.In addition to working as a consultant, Amanda has worked in the corporate environment at big pharma, as well as at a development and commercial manufacturing site, so she can appreciate your particular perspective of the drug development and approval process.

Telephone: +1.435.213.5998
Website: http://arxpharma.com/