After nearly 20 years in the pharmaceutical industry and clinical field, former FDA investigator and Consumer Safety Officer Charisse K. Green is well acquainted with the exacting specifications and numerous requirements presented to companies seeking to enter the business. Through CK Pharmaceutical Consulting Solutions, Green is offering her vast and detailed knowledge on a consulting basis to a select group of companies.

CK Pharmaceutical Consulting Solutions affords your company the opportunity to have a consultant on your team that understands first-hand what the regulators are looking for, one who has worked with numerous foreign regulatory bodies; including MHRA, Swiss Medic, and Health Canada to perform joint inspections including collaboration of inspection reports; and has personally evaluated, assessed and reviewed numerous Quality Management Systems for all FDA commodities. Having held the highest level of FDA certification in cGMP expertise, Green specializes in Biotech and Sterile Aseptic Manufacturing, APIs, pre-approval and GMP inspections.

CK Pharmaceutical Consulting Solutions makes the unparalleled experience of Green’s 15-year FDA career available for the pharma industry. Her multi-faceted agency background uniquely positions her to be able to deliver innovative solutions and extraordinary results for clients globally.