Seminar on Marketing Products without Getting Hammered by FDA at Raleigh | September 17, 2015 9:00 AM - September 17, 2015 6:00 PM | Automation.com

Seminar on Marketing Products without Getting Hammered by FDA at Raleigh

Event Summary

DATE:
September 17, 2015
LOCATION:
Raleigh, NC 27609
COUNTRY:
United States
START DATE/TIME:
September 17, 2015 9:00 AM
END DATE/TIME:
September 17, 2015 6:00 PM
EVENT TYPE:
Training
HOST:
GlobalCompliancepanel
PHONE:
18004479407
EMAIL:
[email protected]
WEBSITE:
Click here to Visit

Description

Overview
With this seminar you will learn how to navigate FDA's legal requirements and its interpretations for enforcement purposes. The agency now applies the principles of cognitive psychology to aid in its determination of what a message really conveys. This becomes a new factor in trying to stay within FDA's legal corral.
This conference will provide insight on how to manage your marketing activity and gauge what regulatory risks your business is willing to accept. You will learn how corporate management requires cooperation between marketing, regulatory affairs, legal counsel, manufacturing, engineering and finance departments. You will understand that a weak link in any department leaves the entire corporation vulnerable to FDA enforcement. Most importantly, you will understand the boundaries that FDA uses and how easy it is to cross them. With information from this course, you can step back and rationally evaluate your firm's regulatory profile for advertising and promotion.
Why you should attend:
If you go "off label" with advertising and promotion, you become embroiled in FDA's advertising and promotion requirements. For devices, the law is weak and lacks legal clarity. For drugs, FDA's law and regulations are extensive and have violated Constitutional protections. Depending on your point of FDA's promotion and advertising requirements can help you or hurt you? There is an inherent conflict in interests. In any case, you need to identify practical criteria to make marketing decisions. That begs the question of whether or not marketing managers and regulatory affairs managers will even try to agree on an issue. FDA's Center for Devices and Radiological Health (CDRH) has never issued a comprehensive guidance on advertising and promotion. You are on your own. CDER has established a pervasive and expanding program. For example, policing social media has become a new regulatory responsibility. Bottom line, do you know when you are running afoul of FDA's requirements or are you guessing? It's become a brooding nightmare for you and consumers.
Areas Covered in the Session:
• FDA's legal authority and Constitutional limitations
• FDA requirements and exemptions
• FDA guidance documents, such as for social media, direct -to-consumer advertising, message formatting and providing risk/benefit information
• Warning Letters
Who Will Benefit:
• Regulatory Affairs
• Quality Assurance
• Manufacturing
• FDA Consultants and Legal Counsel
Agenda:
Day 1 Schedule
• FDA legal authority
o FTC / mass media
o DOJ / False Claims
o FDA application of the FD&C statute and regulations
o False and Misleading
• Cognitive psychology
• Promotion and Advertising: scope of labeling
o Definitions for “label” and “labeling”
 Hard copy and electronic
 Testimonials
 Blogs
 Sales force
o What is “off-label”?
o Practice of Medicine exemption
o Drugs authority
o Devices
o Dietary supplements
• Supreme Court / commercial free speech
o Constitutional protection
o Safe harbor
• Policy
o FDA organizational responsibility
o FDA Guidance
 Balanced disclosure of risk vs. benefit
o Social Media
o Direct to Consumer Advertising
• Hypothetical Workshop
Day 2 Schedule
o Direct to consumer advertising
o Federal Trade Commission authority
o Fair and balanced information
o Context and format
o Script versus message
 Target population
 Aspirations
 Emotional factors
o False and misleading information
 Statutory basis (21 U.S.C. 352(a))
 New use
 Comparative claims
 Claims for safety and effectiveness
 Sales for solicitation
o Off label use
o (Group Hypothetical)
• FDA Warning Letters
• Corporate management responsibility
o FDA - false and misleading
o FTC - false advertising
o DOJ - false claims
Speaker:
Casper (Cap) Uldriks, through his firm "Encore Insight LLC," brings over 32 years of experience from the FDA. As an investigator, he was responsible for countless 483s, scores of Warning Letters, injunctions, individual seizures, mass seizures and was coined by industry as FDA's "Darth Vader." He inspected foods, drugs, methadone clinics and clinical investigators, but specialized in the FDA's medical device program. He served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements for FDA. His comments are candid, straightforward and of practical value.
DATE, VENUE & PRICE:
Location: Raleigh, NC Date: September 17th & 18th, 2015 Time: 9 AM to 6 PM
Venue: Courtyard Raleigh Midtown
Venue Address: 1041 Wake Towne Dr, Raleigh, NC 27609, United States
Price: $1,695.00
Register now and save $200. (Early Bird)
Until August 10, Early Bird Price: $1,695.00
From August 11 to September 15, Regular Price: $1,895.00

Registration Link - http://bit.ly/1OZWzFy

Contact Information:
NetZealous LLC,
DBA GlobalCompliancePanel,
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA
Phone: 1800 447 9407
Fax: 302 288 6884
Email: [email protected]
Website: https://www.globalcompliancepanel.com

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