Why Drug & Dietary Supplement Companies Get Warning Letters: How to Handle and Avoid Them training seminars presented by Online Compliance Panel register now on FindaSeminar.com

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Why Drug & Dietary Supplement Companies Get Warning Letters: How to Handle and Avoid Them  

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Online Compliance Panel   

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Regulatory Affairs managers, directors & Associates, Product safety managers, Compliance Specialists

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Seminar Summary:

Anyone who markets drug or dietary supplement products in the USA should be aware of the seriousness of an FDA Warning Letter and know how best to avoid receiving one. This webinar will provide recent examples of FDA Warning letters to convey an understanding of why companies receive them. Proactive and reactive strategies for responding to FDA Warning letters will be covered in this webinar. (see full course description)

 

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Training Course Syllabus:


Objectives of the Presentation

Learn why OTC & Prescription drug and dietary supplement companies get FDA warning letters
Learn about FDA enforcement priorities for drugs & dietary supplements
Review examples of FDA warning letters that drug & dietary supplement companies have received
Get tips on why drug & dietary supplement firms get warning letters due to illegal label claims and advertising & promotional issues
Get helpful tips on how to avoid warning letters and respond to an FDA Warning Letter if you do receive one
Proactive and Reactive Strategies for Communicating with FDA

Why Should you Attend

This training will focus on why Rx, OTC drug and dietary supplement companies receive FDA warning letters primarily due to claim issues and what steps can be taken to avoid them. Along with examples of warning letters, you will be provided with tips and strategies for communicating with the FDA and how to respond to a warning letter. You will be given the references to all relevant FDA & FTC regulations and guidance documents.

Who will Benefit

Regulatory Affairs managers, directors & Associates, Product safety managers, Compliance Specialists, Regulatory affairs professionals, Senior management executives (CEO, COO, CFO, etc), Dietary supplement manufacturers, marketers, Regulatory compliance associates and managers, Legal and medical experts involved in dietary supplements industry, People investing in FDA-regulated product development projects, Packaging Personnel & Management, Design Personnel & Management, Quality Assurance Analyst & Management, Marketing and Product managers, Drug & Dietary Supplement company attorneys

Seminar Summary:

Anyone who markets drug or dietary supplement products in the USA should be aware of the seriousness of an FDA Warning Letter and know how best to avoid receiving one. This webinar will provide recent examples of FDA Warning letters to convey an understanding of why companies receive them. Proactive and reactive strategies for responding to FDA Warning letters will be covered in this webinar. (see full course description)

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