Jo Maugh, MBA

Ms. Maugh served in Regulatory Affairs and Clinical Quality Assurance positions with major pharmaceutical companies for over 30 years prior to becoming a consultant.  Immediately upon the development of the Good Clinical Practices regulations, Ms. Maugh established and managed the Clinical Quality Assurance department for Marion Laboratories.

Numerous CQA audits of investigators, sponsors, IRBs, clinical laboratories, and CROs for large, multi-national companies as well as small companies, have been successfully conducted by Ms. Maugh.   Regulatory submissions (IND through post-NDA), regulatory review of promotional materials, and CQA experiences range from  the Cardizem® line of products to the Mucinex® line of products.  Writing, implementing, and auditing of SOPs for both Regulatory Affairs and CQA are among her many skills and achievements.