Syner-G BioPharma Group
Libby Russell, PhD, is an accomplished professional in the pharmaceutical and biotechnology industries, currently serving as Vice President at Syner-G BioPharma Group. Previously, Libby held the position of Senior Vice President of Business Development and Senior Consultant at RMC Pharmaceutical Solutions, as well as Senior Vice President at Neva Analytics. Libby's background also includes a role as Associate Director of Commercial Manufacturing at Ophthotech and experience as a Lecturer at the University of Colorado. Educationally, Libby is pursuing a Doctor of Philosophy (PhD) in Chemical Engineering at the University of Colorado Boulder and holds a Master of Science (M.S.) in Chemical Engineering from Tufts University.
This person is not in any teams
This person is not in any offices
Syner-G BioPharma Group
Syner-G BioPharma Group provides in-depth expertise across the three key elements of Chemistry, Manufacturing, and Controls (CMC): Regulatory Services, Technical Development, and Quality/IT. We call this CMC 360™. We also provide medical writing services, with expertise in authoring a variety of regulatory documents across a wide range of therapeutic areas and in all phases of development. Our regulatory affairs services include the development and implementation of global regulatory strategic plans, regulatory agency meeting support, and electronic submissions to regulatory authorities around the world. We have the skill set and experience to guide your prime asset through any development challenges and along the ever-changing maze of regulatory filing pathways, to a position of full compliance, and high quality. Our expertise spans small molecules, peptides, oligonucleotides, biologics, monoclonal antibodies, antibody-drug conjugates, and cell and gene therapy products.