10 Key Steps to Bulletproof CGMP Compliance

This training program will emphasize why U.S. FDA says it's getting tougher. This 10-key steps program will teach attendees to be ready and compliant. Recent events and audits indicate the past ways of doing things is not acceptable. The agency continues to use high-profile cases to drive compliance to smaller companies and suppliers.

Why Should You Attend:

"Business as usual" is unacceptable. Once model companies have fallen flat or worse. Don't let your company be caught off guard by these major shifts in emphasis. Enhance awareness and modify internal audits to match this FDA shift.

Who Will Benefit:

This webinar will provide valuable assistance to all regulated companies in evaluating their existing compliance and internal audit emphasis in light of the changes in the FDA's CGMP audit paradigm. The information within applies to personnel / companies in the pharmaceutical, medical device, diagnostic, and biologics fields. The employees who will benefit include:

Senior Management

Regulatory Affairs

Quality Assurance

Production

Engineering

Instructor Profile:

John E. Lincoln is principal of J. E. Lincoln and Associates LLC, a consulting company with over 33 years' experience in U.S. FDA regulated industries, 19 of which are as an independent consultant. He has worked with companies from start-up to Fortune 100 in the U.S., Mexico, Canada, France, Germany, Sweden, China and Taiwan. 

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/10-key-steps-to-bulletproof-cgmp-compliance-webinar-training-704250-prdw?channel=sciencedz