Stanley Alekman, Ph.D.
Independent Pharmaceutical Consultant
He is a pharmaceutical consultant for more than 35 U.S. and foreign generic and PhRMA pharmaceutical firms since 1998, including consent decree remediation programs
A record of accomplishment in QA and QC; laboratory operations; regulatory compliance; R & D, and mfg management in the chemical and pharmaceutical industries
Extensive interaction with FDA at the District, Center – PQRI and AAPS committee activities; Member of ASTM E-11 and E-55 Quality Control and Statistics, and Pharmaceutical and Biopharmaceutical Manufacturing Technology committees Effective coach, mentor and trainer.
