CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019

  • 12 Jun 2019
  • Webinar

Description

CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019 is a webinar dedicated to "Learn 21 CFR subpart J of FDA regulations related to CAPA, how to integrate CAPA with other branches of QMS.

CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019 covers topics such as:

  • Responsibilities of manufacturers
  • Get an in-depth understanding of what regulatory agencies such as the FDA are requiring for CAPA.
  • Documentation requirements
  • Evaluate your already-existing CAPA process to determine if it meets requirements.
  • Overview of commonly-used root cause analysis functions.
  • Determine if your CAPA system is robust enough to ensure actions are effective or overly-complicated and preventing smooth operation.
  • Tips and tricks for implementing a successful CAPA system.
  • Understand some misconceptions with CAPA implementation.

CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019 intended for:

  • Regulatory Affairs
  • Quality assurance
  • Managers
  • Quality Control Directors
  • Regulatory Compliance Directors

Past Events

Important

Please, check "CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance
Education: Training
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Medical laboratories, Medical technology, Pharma

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