LES SCHNOLL


Les Schnoll is the senior director for quality systems at the biopharmaceutical company Theravance Inc. He's a member of the U.S. TAG to ISO/TC 176 and ISO/TC 210, and has more than thirty years of experience in quality assurance and control, auditing, and regulatory compliance in the medical device, pharmaceutical, and clinical/preclinical laboratory, industrial, and food industries. He's the author of The Regulatory Compliance Almanac and The CE Mark: Understanding the Medical Device Directives.


The CE Mark: Understanding the Medical Device Directives
The CE Mark: Understanding the Medical Device Directives
The Regulatory Compliance Almanac
The Regulatory Compliance Almanac