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Effective Pharmaceutical GMP Audits and Self-Inspections

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Category gmp training, cgmp training, gmp good manufacturing practice , gmp guidelines for pharmaceuticals, gmp training courses, gmp training materials, GMP Auditor in Pharma companies, Pharmaceutical GMP auditing, GMP compliance training, GMP auditor roles and responsibilities, Pharmaceutical GMP regulations, pharma good manufacturing practices, pharmaceutical regulations compliance, pharma compliance, GMP auditor roles and responsibilities, GMP auditing

Deadline: December 06, 2017 | Date: December 07, 2017

Venue/Country: Online, U.S.A

Updated: 2017-11-14 21:55:01 (GMT+9)

Call For Papers - CFP

Regulators expect audits and self-inspections of the manufacturer to assure the quality of its own operations and those of its suppliers and contractors via repeated audits. FDA and other regulators have contributed to and endorsed ICH Q10, Pharmaceutical Quality System, which explicitly recommends audits as a key element in the review of process performance and product quality and also in the management of outsourced activities and purchased materials.

Objectives of the Presentation:

Understand the GMP context for pharmaceutical quality system lead auditors

Plan, conduct, report and follow-up an audit of a GMP PQS

Provide guidance for auditors of suppliers, contractors, CMO service providers, outsourced activities and self-inspectors

Drive continuous improvement of systems and processes

Drive continuous improvement of auditors and audit systems

For Registration:

Note: Use Promo Code HYED6Z and get 10% off on registration (Valid till DECEMBER 31st 2017)

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