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9 July 2013 -- The Regulatory Affairs Professionals Society (RAPS) will host a webcast, tomorrow, 10 June, at 12:00 pm EDT, covering risk management principles in governance of product and process quality.
The RAPS webcast Developing and Implementing a Risk-Based Quality Program shows how to apply risk management principles to all aspects of product and process lifecycle—from development to routine manufacture. Participants will learn how to develop and launch comprehensive risk management programs and get the tools to integrate risk management into operations. Experts Chris Watts and David Tiffany of NNE Pharmaplan will lead the webcast.
Who:
• Chris Watts, partner, NNE Pharmaplan
• David Tiffany, senior consultant, NNE Pharmaplan
What:
90-minute webcast entitled Developing and Implementing a Risk-Based Quality Program
When:
10 July, 12:00–1:30 pm EDT
How to Access:
Members of the working media may request access to this live RAPS webcast or to the recording by contacting Zachary Brousseau, senior manager, communications, RAPS, at zbrousseau@raps.org or +1 301 770 2920, ext. 245.
About RAPS
The Regulatory Affairs Professionals Society (RAPS) is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products. Founded in 1976, RAPS helped establish the regulatory profession and continues to actively support the professional and lead the profession as a neutral, non-lobbying nonprofit organization. RAPS offers education and training, professional standards, publications, research, knowledge sharing, networking, career development opportunities and other valuable resources, including Regulatory Affairs Certification (RAC), the only post-academic professional credential to recognize regulatory excellence. RAPS is headquartered in suburban Washington, DC, with offices in Europe and Asia, and chapters and affiliates worldwide. RAPS.org
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