Beschreibung
e-Learning: EU GMP Guideline Chapter 8 | Complaints and Product Recall
Managing Risks Before They Become Issues
- Best practices for handling complaints and product recalls
- Implementing corrective and preventive actions (CAPA)
Proactive risk management is key to maintaining GMP compliance. This module details the requirements of EU GMP Guide Chapter 8, covering complaints handling and recall procedures.
At the end of the module you may complete a short assessment. If you reach a passing score of at least 80%, you will receive your certificate via email.
Module language: English
Content
- Principles
- Personnel
- Procedure for investigation
- Root Cause Analysis and CAPA
- Product recall
- Qualified person for pharmacovigilance (Stufenplanbeauftragter)
- Documentation and reporting obligations
Audience
- Employees of quality units
- Employees who process complaints, quality defects and product recalls
Features
- Interactive exercises
- Self-paced learning right at your workplace
- Glossary of helpful terms and explanations
- Suitable as initial training, but also as refresher training or follow-up training
- With certificate
Industries
- Pharmaceuticals
- Active Ingredients
- Contract Manufacturers
Individual solution
This e-learning module can also be customized by our learning engineer team for your company with your internal information (e.g. contact details), content (e.g. organizational charts, schedules, forms, leaflets) and your corporate identity. Feel free to contact us!
License
Single license with a 365 day term.
e-Learning: EU GMP Guideline Chapter 8 | Complaints and Product Recall
