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

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

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

Future Events

CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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