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    Quality Management and Quality Audit According to GxP/GMP Requirements

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    Website https://www.complianceonline.com/quality-management-and-quality-audit-according-togxp-gmp-requiremen | Want to Edit it Edit Freely

    Category

    Deadline: April 26, 2019 | Date: April 26, 2019

    Venue/Country: U.S.A

    Updated: 2019-04-03 20:50:40 (GMT+9)

    Call For Papers - CFP

    GxP/GMP is about Quality Management System (QMS) where an organization needs to demonstrate its ability to consistently provide product that meets customer and applicable statutory and regulatory requirements.

    There are few types of quality audits. One of them is GMP audit. GMP audit is very important and critical for an organization in a regulated industry. The preparations for the audit should be done properly before the audit. The primary objective of the audit is to demonstrate the compliance with GxP/GMP regulations. FDA can drop in anytime to perform an unannounced GMP audit or investigation. A GMP audit is conducted to check whether your organization complies with GxP/GMP and to identify if you have full control over your processes, facility, and quality management system (QMS).

    Learn about GxP/GMP regulations and how they affect quality management system and quality audit. Learn about different types of quality audits and how to properly prepare for them, what actions you need to take to ensure that your organization will pass an audit.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.