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The original message has been attached to this so you can view it or label similar future email. If you have any questions, see root\@localhost for details. Content preview: FDA Scrutiny of Promotion and Advertising Practices Your Gateway to Regulatory Compliance View Online About Us Webinars($10) Seminars Past Seminar Pictures Use MGCP50 Promo Code to GET FLAT 50% OFF on ALL SEMINARS - Offer Ends Today 2-day In-person Seminar FDA Scrutiny of Promotion and Advertising Practices Click Here for More Details! Overview: If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue. Advertising and promotion for devices is weak and lacks legal clarity. For drugs, the regulations are prescriptive and guidance documents clamp down on nuances. Marketing and regulatory affairs departments must collaborate to avoid the hammer and penalties of FDA. The roadblock, however is that marketing managers and regulatory affairs managers rarely reach common ground and are loathe to even consult with each other. Read more... Date & Time Date: May 17th & 18th, 2018 Time: 9:00 AM to 4:30 PM Download Seminar Brochure Venue Philadelphia, PA DoubleTree by Hilton Philadelphia Airport Download Registration form Casper Uldriks ex-FDA Expert and former Associate Center Director of CDRH Casper (Cap) Uldriks, owns Encore Insight LLC, which provides consulting services on FDA Law. He brings over 32 years of experience from the FDA. He specialized in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and as an Associate Center Director for the Center for Devices and Radiological Health. Reserve your Seat Now Enroll Now! GlobalCompliancePanel 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Fax: 302 288 6884 www.globalcompliancepanel.com | Unsubscribe Copyright © 2017 GlobalCompliancePanel. All rights reserved. [...] Content analysis details: (1.6 points, 3.0 required) pts rule name description ---- ---------------------- -------------------------------------------------- 0.0 URIBL_BLOCKED ADMINISTRATOR NOTICE: The query to URIBL was blocked. See http://wiki.apache.org/spamassassin/DnsBlocklists#dnsbl-block for more information. [URIs: globalcompliancepanel.com] -0.0 SPF_PASS SPF: sender matches SPF record 0.0 HTML_MESSAGE BODY: HTML included in message 0.7 MIME_HTML_ONLY BODY: Message only has text/html MIME parts -0.0 BAYES_20 BODY: Bayes spam probability is 5 to 20% [score: 0.0691] -0.1 DKIM_VALID_AU Message has a valid DKIM or DK signature from author's domain 0.1 DKIM_SIGNED Message has a DKIM or DK signature, not necessarily valid -0.1 DKIM_VALID Message has at least one valid DKIM or DK signature 1.0 FROM_EXCESS_BASE64 From: base64 encoded unnecessarily X-Spam-Flag: NO <=21DOCTYPE html PUBLIC =22-//W3C//DTD XHTML 1=2E0 Transitional//EN=22 =22h= ttp://www=2Ew3=2Eorg/TR/xhtml1/DTD/xhtml1-transitional=2Edtd=22> FDA Scrutiny of Promotion and Advertising Practices <=21-- START OF PRE-HEADER A= REA BLOCK-->
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Your Gateway to Regulatory Compliance View Online
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About Us Webinars(=2410) Seminars
Past Seminar Pictures
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Use MGCP50 Promo Code to GET FLAT 50% O= FF on ALL SEMINARS - Offer Ends Today
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2-day In-person Seminar
FDA Scrutiny of Promotion and Advertising Practices
Click Here for More Deta= ils=21
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Overview: If you go =22off label= =22 with advertising and promotion, FDA's hammer can hit hard and seemingly= out of the blue=2E Advertising and promotion for devices is weak and lacks= legal clarity=2E For drugs, the regulations are prescriptive and guidance = documents clamp down on nuances=2E Marketing and regulatory affairs departm= ents must collaborate to avoid the hammer and penalties of FDA=2E The roadb= lock, however is that marketing managers and regulatory affairs managers ra= rely reach common ground and are loathe to even consult with each other=2E = Read more=2E=2E= =2E
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= Date & Time
Date: May 17th & 18th, 2018
Time: 9:00 AM= to 4:30 PM
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= Venue
Philadelphia, PA
DoubleTree by Hilton Philadelp= hia Airport
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= Casper Uldriks
ex-FDA Expert and former Associate Center Direct= or of CDRH
Casper (Cap)= Uldriks, owns Encore Insight LLC, which provides consulting servi= ces on FDA Law=2E He brings over 32 years of experience from the FDA=2E He = specialized in the FDA's medical device program as a field investigator, se= rved as a senior manager in the Office of Compliance and as an Associate Ce= nter Director for the Center for Devices and Radiological Health=2E<= /td>
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Reserve your Seat Now
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Enroll N= ow=21
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GlobalComp= liancePanel
161 Mission Falls Lane, Suite = 216, Fremont, CA 94539, USA=2E
Phone: +1-800-447-9= 407
Fax: 302 288 6884<= /td>
www=2Eg= lobalcompliancepanel=2Ecom =7C Unsubscribe
Copyright © 2017 GlobalCo= mpliancePanel=2E All rights reserved=2E
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