NSF Health Sciences Ltd.
Lynne Byers has over 35 years’ experience in manufacturing management and QA of a wide range of sterile and non-sterile dosage forms, and is fully conversant with current EU and FDA GMP regulations and requirements.
She has extensive experience in international QA auditing of a wide range of pharmaceutical manufacturers who are suppliers to the pharmaceutical industry worldwide. She also has extensive experience in managing QA teams in country affiliates.
Lynne also worked as Head of Inspectorate and Licensing for the MHRA from 2004-2006 and joined NSF in 2017.