"Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration"
Website www.compliance2go.com |
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Category Biotechnology , Medical Device
Deadline: August 27, 2014 | Date: August 27, 2014
Venue/Country: Houston, U.S.A
Updated: 2014-07-28 19:08:09 (GMT+9)
Call For Papers - CFP
DESCRIPTIONAll life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records.Life science manufacturing plants have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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