Live -Webinar 2014 - Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
Topics/Call fo Papers
DESCRIPTION
All 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.
All 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.
Other CFPs
- FDA 510(k) Update: Trends, New Strategy, Submission and FDA Clearance
- Maintaining a Validated State ? PV, PM and Statistics associated with Current Regulation
- ITR- International Conference on Mechanical And Production Engineering
- ITR-International Conference on Electrical Electronics and Data Communication
- ITR- International Conference on Advanced Computer Science and Information Technology
Last modified: 2014-08-18 20:50:41