FDA Audit, Quality Assurance Practices, Responsibilities and Expectations

  • Sep 2020
  • United States

Description

FDA Audit, Quality Assurance Practices, Responsibilities and Expectations is a conference that covers topics such as:

  • Quality areas that are the point of focus during regulatory, corporate or third party audits
  • Regulatory expectations of the quality unit and its role in the Quality System Requirements (QSR)
  • The importance of training, its documentation, and common concerns being raised over "operator error"
  • Typical checklist that can be used as a template for the performance of audits
  • The current focus on data integrity issues and the current guidance document regarding it
  • The importance and regulatory guidance offered for the investigation of deviations/out-of-specification results
  • Weaknesses of each person`s current quality system and possible recommended corrective actions
  • Top 10 most commonly cited drug GMP deficiencies for 2015-2016

FDA Audit, Quality Assurance Practices, Responsibilities and Expectations brings together:

  • Quality professionals
  • Senior quality managers
  • Compliance professionals
  • Regulatory professionals
  • Manufacturing engineers
  • Production supervisors
  • Design engineers
  • Production engineers
  • Quality engineers
  • Process owners
  • Document control specialists
  • Quality auditors

Past Events

Important

Please, check "FDA Audit, Quality Assurance Practices, Responsibilities and Expectations" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical technology, Pharma
Science: Life Sciences & Biology
Technology: Biotechnology

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