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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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November 07, 2008 |
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Centre for Applied Training and Development, London, UK
2009-03-16 & 2009-03-17
This two-day training course will guide and develop your understanding of: · Regulatory Requirements for CAPAs and OOS Investigations· Secure Strategies for Compliance · How to Maximize Benefits from CAPAs and OOS Investigations · How to Manage Typical Issues that Arise Both FDA and European Regulators expect pharmaceutical products manufacturers to have in place a system for CAPA to correct process deficiencies and maximise process improvement. In addition, manufacturers must have a secure system for management of Out of Specification Results (Non-Conformances) to ensure that all product on the market is safe and meets its registration requirements.
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Organized by:
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Centre for Applied Training and Development |
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Invited Speakers:
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info@catdglobal.com
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Deadline for Abstracts:
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n/a
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Registration:
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Please refer to the register tab on the CATD website (www.catdglobal.com) or click on the title of the course on the conferences/meeting or home page to register on line.If you have any problem registering please do not hesitate to contact us at info@catdglobal.com or call us at + 44 (0) 20 8485 1234 or fax us at + 44 (0) 20 8485 1234
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E-mail:
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info@catdglobal.com
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