Seminar & Resource Kit Details
FDA GMP Enforcement Trends and Priority Inspection Areas
CD includes the one-hour presentation and Q&A session with attendees plus all the individual slides, reference material and customizable training certificate. Speaker: John Avellanet. Event ID: 664612
Summary
Tougher investigations and enforcement penalties are on the rise, particularly with the new powers to levy fines granted to the FDA by the FDAAA 2007. Pharma, biotech and device executives are being held accountable even if they did not participate in or know about the wrong-doing.
This seminar will help you spot the red flags in your organization before the inspector comes knocking.
Based on discussions with FDA officials, plus the suggestions of clients and members of the SmarterCompliance Toolkit program, this recorded seminar is full of the critical information you need to stay out of the crosshairs of the FDA for the next 2-3 years.
Is your company on the list for inspection this year?
You will learn:
The three new business-critical areas the FDA is turning its eye upon
What your recall policies must address - and measure - at all costs
What the inspector will examine when it comes to your CAPA and MDRs
Current FDA targets and priorities
Red flags the inspector looks for based on your type of company
Recent enforcement actions and FDA expectations
What the FDA wants to see when it comes to your quality systems plan priorities
And much more
On the CD:
Customizable training certificate
Printable speaker's slides
Synchronized audio recording of the presentation and Q&A session
Industry report: FDA Enforcement Trends and Recommendations 2008-2009
And more
This information-packed recorded seminar will help see your firm with the inspector's eyes with advice straight from the FDA. You will never again worry about the knock on the door.
Your purchase also includes a complimentary six-month trial to the SmarterCompliance newsletter of FDA intelligence, practical quality systems advice, and regulatory compliance analysis ($144 value).
About the Presenter
John Avellanet is a well-known leader in lean compliance and quality systems management. He is a frequent and sought-after speaker for corporate management workshops, trade association conferences, business schools, and forums such as FDAnews, FOI Services, PharmaQbD, the Management Roundtable, and Expert Briefings. He publishes the monthly executive newsletter, SmarterCompliance™, has written more than 30 articles syndicated in biopharmaceutical and device journals world-wide, and is a co-author of the book, Best Practices in Biotechnology Business Development. Many of his clients and SmarterCompliance™ subscribers view him as their senior compliance and quality advisor.
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Additional Details
The purchase price for the recorded seminar is $325 USD (shipping is free). We accept MasterCard, Visa, Discover, and American Express through PayPal for online payment.
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