- email:registration@pti-europe.co.uk
- phone:+44 (0) 20 7017 7481
 |
Mastering your Performance as a QA Professional
22 - 23 August 2012, REGUS, One Embarcadero, San Francisco, USA
|
Mastering Your Performance as a QA Professional
Course Objectives
This course clarifies the roles and expectations of Quality Assurance throughout the entire process, from development of quality systems through internal audits and agency inspections.
- Evaluate the current regulatory environment, ensure compliance and address vulnerable areas.
- Review current hot topics within the quality arena including: CAPA, complaint handling, validation responsibilities, batch record review and change control.
- Attend the most comprehensive and interactive QA course available to maximize your quality skills and improve your daily job performance.
What Will You Learn?
- Carry out the full range of QA responsibilities read more
- Complete internal audits read more
- Properly investigate deviations read more
- Conduct Root Cause Analysis read more
- Prepare for a systems-based cGMP read more
- Avoid compliance issues read more
- Establish an efficient QA system read more
- Implement and maintain an effective change control program read more
- Conduct batch record reviews read more
Why you should attend
Quality Assurance is critical to the successful development and manufacture of products and the maintenance of regulatory compliance. This two-day course is designed to improve your on-the-job performance as a GMP QA professional by providing systematic instruction on vital skill sets.
Who Should Attend
This introductory to intermediate-level course is designed for Pharmaceutical, Biotechnology and Medical Device professionals. Specifically, individuals with the following titles would benefit most from the course:
• QA Associate/Specialist/ Manager
• Quality Systems Manager
• QC Specialist
• Laboratory Manager
• GMP Compliance Specialist
• Regulatory Affairs Associate/Manager
• Audit Services Manager
• Quality Engineer
• Production Manager
• Manufacturing Supervisor
• Validation Engineer
• Compliance Manager
• Systems Manager
• Documentation Specialist
Reviews
No reviews
Related Events
Introduction to Good Manufacturing Practices (GMPs)
20 Sep 2012 - 21 Sep 2012
REGUS Overlook Princeton, New Jersey, USA
Writing Standard Operating Procedures
23 Aug 2012 - 24 Aug 2012
Regus Soma- San Francisco, California, USA
Feeds | Like | Share    |
Dates and Venues
22 Aug 2012 - 23 Aug 2012
REGUS, One Embarcadero, San Francisco, USA
04 Dec 2012 - 05 Dec 2012
REGUS, One Embarcadero, San Francisco, USA
Connect with the PTI faculty! PTI is a global pharmaceutical training company with over 60 interctive courses focusing on Regulatory Affairs, R&D, Clinical, Business Strategy, Fine Chemicals, Biopharmaceuticals, Manufacturing, Medical Devices and Agrochemicals
Follow PTI on twitter:
@PTI_Courses
