FACILITY VALIDATION & QUALIFICATION

Venue: Hilton Toronto Airport

Location: Mississauga,, Ontario, Canada

Event Date/Time: Nov 14, 2005 End Date/Time: Nov 15, 2005
Report as Spam

Description

Successful Strategies and Best Practices for Ensuring Regulatory Compliance of Pharmaceutical & Biopharmaceutical Manufacturing Facilities

A ONE & HALF A DAY COMPREHENSIVE & INTERACTIVE COURSE & WORKSHOP ON:

- Regulatory Requirements on Facility Qualification
- Qualification of Critical Utility Systems
- Design, Commissioning and Validation of HVAC Systems
- Design and Commissioning of Pharmaceutical Water Systems - Complying with USP, EP and FDA Requirements
- Specific requirements for Clean Steam
- Assigning Qualification levels for equipment/system
- Effective Design Qualification
- Change Control Management for Facility Design and Qualification
- Commissioning and Qualification for Classified Environments
- Determining Effective and Practical Facility, Utilities and Equipment Qualification Levels Using Risk Assessment
- Commissioning Procedures for New Manufacturing Facilities

AND MUCH, MUCH MORE

DISTINGUISHED SPEAKERS & MODERATORS

Mr. Miguel Montalvo
Mr. David W. Vincent

Who Should Attend?

Because of its comprehensive content, this course will be most valuable to Directors, Managers, Supervisors, Analysts, and Associates in the Pharmaceutical, Biotechnology, Vitamin, Herbal, and allied industries with daily responsibilities in the following areas:

- Validation
- Quality Assurance
- Change Control
- Project Management
- Production
- Engineering
- Facility Monitoring
- GMP/GLP Compliance
- Regulatory Affairs
- Product Submission
- Training
- Documentation and Technical Writing
- Contract Laboratories
- Consultants
- Contract manufacturing

Others who interact together to launch a product

Venue

5875 Airport Road
Mississauga,
Ontario
Canada
MORE INFO ON THIS VENUE

Types