- Translated with AI
Current Topics in Cleaning Validation
Proven methods and procedures for better cleaning validation, compliance, and quality control
Cleaning and cleaning validation are key components of GMP manufacturing. STERIS Life Sciences offers a series of one-day seminars "Current Topics in Cleaning and Cleaning Validation" in Europe, illustrating how to apply the principles of FDA guidance in process validation and EU GMP Annex 15 (revised) for cleaning validation. This seminar will also address various current challenges in the pharmaceutical and biopharmaceutical industries.
Workshop Content:
- GMP manufacturing of safe and effective medicines
- Clarification and application of the principles of FDA guidance on process validation and EU GMP Annex 15 (revised) for cleaning validation
- A lifecycle approach to comprehensive cleaning validation
- Application of health-oriented limits in cleaning validation
- Discussion of "rings" in buffer preparation containers
- Challenges of dealing with biofilm
Target Audience:
- Quality assurance
- Regulatory authorities
- Plant management
- Quality control
- Production
- Compliance
- Microbiology
- Facilities/Maintenance
- Engineering
Date: March 10, 2015
Location: Dormero Hotel Stuttgart, Plieninger Straße 100, 70567 Stuttgart, Germany
Contact: Andrea Haselmayr: andrea_haselmayr@STERIS.com
Register Online at: http://www.sterislifesciences.com/News-and-Events.aspx
STERIS Deutschland GmbH
50933 Köln
Germany
