Schedule a meeting with Brandon Butler
Attending DIA? LMK will be featured at DIA in booth #741. Come by our booth to meet with one of our TMF consultants, Brandon Butler, or use this form to set up a meeting with us and learn how we can help make your TMF better.
Prior to joining LMK Clinical Research, Brandon spent nearly 8 years managing quality assurance and environmental inspection of sterile compounding facilities in accordance to FDA and State Boards of Pharmacy requirements. Brandon has expert knowledge of GDP, cGMP and USP <797>, and he holds several industry specific certifications. He has advised some of the world’s largest pharmaceutical manufacturers and leading hospital systems of cleanroom performance and design. Brandon transitioned his compliance expertise to the front end of drug development in 2015.