Christopher Markos, MS

Chris Markos provides chemistry, manufacturing, and controls (CMC) regulatory affairs and quality assurance support to the healthcare products industry.  His experience includes pharmaceuticals (Rx and OTC), dietary supplements, cosmetics, and medical devices.  Chris specializes in developing and implementing regulatory CMC strategies for investigational and commercial products in global markets, including oral, injectable, and topical dosage forms.  Additionally, his experience includes regulatory writing and submission support, quality assurance support, and scientific/regulatory issue research and analysis.  Prior to working in CMC Regulatory Affairs, Chris worked in a drug product manufacturing facility as well as in technical support and R&D.  Chris has a Graduate Certificate in Regulatory and Quality Compliance (RQC) from Purdue University, a Master’s Degree in Management from Northwestern University, and a B.S. in Engineering from the University of Illinois at Urbana-Champaign.