Fullerton, CA – On November 20, 2015 at 10:00 AM PT, industry-expert speakers will address the changing landscape of USP guidelines affecting compounding pharmacies. Terra Universal’s webinar will cover topics including DQSA compliance, designing cleanrooms to meet USP 800 hazardous drug compounding, and cleanroom cost estimating.
Oversight over 503(a) and 503(b) pharmacies has shifted from State Boards of Pharmacy to the FDA. The overlap of authority has become a source of uncertainty for many health professionals. The webinar speakers will provide an overview of the requirements and how they apply to various classes of pharmacies. Cleanroom design and expected expenses will also be covered.
Speaking will be Chris Munoz, PharmD and Principle Consultant for ITL Consulting, a firm specializing in pharmacy business and regulatory affairs. Joining him is Jesse Martinez, PharmD, FASCP and Vice Dean of the College of Pharmacy for Western University of Health. Both speakers are pharmacists, remain active in industry associations, and have worked for, and with, pharmacies and pharmaceutical companies.
Registration for the November 20, 10 AM PT website can be completed by visiting this link: http://bit.ly/1l84svy. Registrants will receive the white paper "Designing your Compounding Cleanroom for USP/cGMP Compliance."