Richard Friedman, Associate Director, Office of Compliance, CDER, FDA will present Regulatory Expectations – Pharmaceutical Manufacturing at the PDA Education Program taking place at INTERPHEX 2014. Friedman’s presentation is a part of the Industry Trends and Regulatory Expectations Session on March 18, 2014 from 10:45am-12:15pm. This session will bring regulators and industry together to discuss expectations and explore trends focused on the use of technology, risk based decision making, process capability, and quality systems needed to achieve the objective of manufacturing excellence. Find out more about the PDA Education Program and register to attend at www.INTERPHEX.com/PDAEducation.
About INTERPHEXINTERPHEX, sponsored by PDA (Parenteral Drug Association), is the single source for complete biopharmaceutical manufacturing solutions to safely and cost effectively process all dosage forms for life-enhancing drugs. It brings over 10,000 global pharmaceutical and biotechnology professionals together with 625+ suppliers through a unique combination of exhibition, education, workshops, partnering opportunities, and networking events.
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