Deviation and CAPA Best Practices Training
Deviation/CAPA training module.
2 000 Skr
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Purpose:
Provides structured training content on best practices for the identification, documentation, investigation, and management of deviations and corrective and preventive actions (CAPA) within a GMP quality system.
Regulatory Alignment:
Aligned with EU GMP requirements for deviation management and CAPA, including expectations under the Pharmaceutical Quality System as described in ICH Q10.
Included Files:
• Deviation and CAPA best practices training material
• Overview of deviation classification and root cause analysis concepts
• Practical examples and discussion points for GMP application
Format:
Microsoft PowerPoint or Microsoft Word (fully editable)
Intended Users:
Pharmaceutical manufacturers, quality assurance teams, quality control, manufacturing, and technical personnel involved in deviation and CAPA management.