The International Regulatory Affairs Network
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
19.04.2010 - 21.04.2010
Ort: Dublin, Ireland
This course will provide the participant with knowledge of current GMPs, how they are applied in the Bio/Pharmaceutical market today, and how they will be enforced in the future.
This three-day course is designed for those who work in a current Good Manufacturing Practices (cGMP) environment and whose roles and responsibilities require that they understand and apply cGMP Quality principles. This course is intended to give participants a thorough understanding of cGMP principles, as well as, tools that may be used in developing and managing current Good Manufacturing Practices. Pictures, flow diagrams, examples of actual procedures and warning letters are included in the presentation to demonstrate basic cGMP concepts. Participant interaction is desired and encouraged.
E-Mail
http://www.cfpie.com/showitem.aspx?productid=095&source=swissbio
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