Learn more about FDA’s current audit techniques and the most commonly cited GMP deficiencies that you have to watch out for. The webinar instructor, an FDA and GMP training expert, will help attendees analyze a system of risk assessments to determine audit frequencies.
Why Should You Attend:
The success of an audit by federal regulators does not always depend on the level of training proffered to staff and department employees, but also in understanding the focus of recent inspections within the industry. Such information provides a template for companies to analyze their own practices and ensure similar issues have been adequately addressed. In addition, as the audit techniques of the FDA have changed over the years, knowing what to expect can help establish a focused training program as part of the preparation.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in:
Quality assurance
Quality control
Manufacturing
Validation
Production
Regulatory compliance
Instructor Profile:
Kenneth Christie has over 30 years of sterile manufacturing and regulatory GMP consulting experience in the areas of quality assurance and validation management in the pharmaceutical and biotechnology industries. Mr. Christie is currently the chief operating officer for VTS Consultants, Inc., located in Amhesrt, MA. His responsibilities specifically include quality system auditing, GMP training, and serving as a subject matter expert for aseptic manufacturing processes, medical devices, APIs and solid dosage processing equipment, utilities, and systems on a global basis. He also performs vendor audits, site pre-approval inspections and assists clients with addressing and correcting regulatory observations.
Note:
Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.
For Registration:
http://www.complianceonline.com/current-fda-audit-practices-and-most-cited-gmp-deficiencies-webinar-training-703635-prdw?channel=sciencedz