"Batch Production Record and Device History Record Review and Quality Assessment"
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Deadline: August 13, 2014 | Date: August 13, 2014
Venue/Country: Houston, U.S.A
Updated: 2014-07-28 19:06:02 (GMT+9)
Call For Papers - CFP
DESCRIPTIONTypical Elements Required to be Included in the Batch Production Record and the Device History Record in order to Accomplish a Quality and Cost Effective Review and Quality Assessment based on current Regulatory Expectations.Why should you attend A vast majority of the current industry deficiencies which have led to isolated 483s, Warning Letters and Consent Decrees are the result of deficient technical documentation of the production processes for both injectables, devices and solid dosages.Quality Systems require both Operations and Quality Departments to be unified with the overall intent of minimizing patient risk by documenting the process in a fashion that is technically accurate and easy to demonstrate that we are thinking and operating with the same objectives as the regulatory agencies are required to enforce For any assistance contact us at?support
compliance2go.com?or call us at?877.782.4696 Or Visit us:- https://compliance2go.com/product/?pid=CP2014-342
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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