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    HEALTHCARE TRAINING 2021 - 6-Hour Virtual Seminar on GxP/GMP and its Consequences for Quality Management, Quality Audit, Documentation, and Information Technology Systems

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    Website https://gcplearning.com/virtual-seminar/6-hour-virtual-seminar-on-gxp-gmp-and-its-consequences-for-q | Edit Freely

    Category HEALTHCARE TRAINING 2021

    Deadline: August 04, 2021 | Date: August 04, 2021

    Venue/Country: Online event, U.S.A

    Updated: 2021-07-02 20:54:18 (GMT+9)

    Call For Papers - CFP

    GxP/GMP regulations are required to be used in regulated industries such as food, pharmaceutical, medical devices, and cosmetics. GMP regulations describe required quality management system for production and testing of products in these regulated industries. The purpose of the GMP regulations is to ensure that a product is safe and meets its intended use.

    Quality management system ensures that a product is safe and meets its intended use. Quality management system has four main components: quality planning, quality assurance, quality control, and quality improvement.

    Quality audit is the process of systematic inspection of quality management system which is carried out by an internal or external auditor or an audit team. It is an important part of organization's quality management system and is the major part of GxP/GMP regulations.

    In this webinar, the framework of GxP/GMP regulations, quality management system, and quality audit will be described.

    Documentation is a critical tool for ensuring GxP/GMP compliance.

    In the regulated environment which must be GxP/GMP compliant, document control is the cornerstone of the quality system. It is so important that if an external audit identifies deficiencies in the document control system, the entire organization can be shut down.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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