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Combination Products: How To Get Your Combination Product Approved And Onto The US Marketplace
Combination Products: How To Get Your Combination Product Approved And Onto The US Marketplace
This course is useful for professionals who have Combination Products or are planning to have these at some point of time in the future.
Fremont,
California,
United States
(sardnews.org)
17/07/2014
Summary: GlobalCompliancePanel will organize a RAPS-approved two-day, in-person seminar in Philadelphia, PA on the topic, “Combination Products: How To Get Your Combination Product Approved And Onto The US Marketplace” on July 17 and 18, 2014 (Thursday & Friday). The speaker at this two-day session is Albert A. Ghignone, CEO of AAG Inc.
This course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
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Venue, date and timings: The venue for this seminar, which will be on July 17 and 18, 2014 from 9 A.M to 6 P.M EDT, is Hotel DoubleTree by Hilton Hotel Philadelphia Center City, 237 South Broad Street, Philadelphia, Pennsylvania, 19107-5686.
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What the seminar is about:
This course is useful for professionals who have Combination Products or are planning to have these at some point of time in the future. The speaker will explain the entire FDA Combination Product system and how to navigate the FDA Combination Product system. For those organizations that want to get a Combination Product out into the US marketplace; this course is of high value.
This is how the speaker at this course will proceed: He will provide a comprehensive understanding of the FDA Combination Product system, which will act as a foundation of knowledge for participants about the FDA Office of Combination Products, the FDA Combination Product system, and Combination Product submissions. He will also explain the scientific and regulatory principles involved.
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About the Speaker:
Albert A. Ghignone MS, RAC is the CEO of AAG Incorporated. For more than 30 years his focus has been on FDA related matters in regulatory affairs, quality assurance and clinical affairs. He has expertise in dealing with all aspects of the FDA approval process for drugs, biologics, medical devices and generic drugs.
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For whom:
This seminar will benefit professionals in:
o Regulatory Affairs Personnel
o Research Personnel
o Quality Personnel
o Clinical Personnel
o Manufacturing Personnel
o Personnel who require an understanding of the FDA Combination Product Process
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About GlobalCompliancePanel:
GlobalCompliancePanel (GCP) is a specialized offering from NetZealous LLC, a Technology and Business Process Solutions and Services Company registered in Fremont, CA. It is a fountainhead for Continuous Professional Education, compliance training and consulting.
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Price:
Register now and save $200. (Early Bird)
Until July 4: Early Bird Price: $1,295.00.
From July 5 to 15: Regular Price: $1,495.00
Discounts are available for group participation in the following manner:
For two attendees: 10% discount
For three to six attendees: 20% discount
For seven to 10 attendees: 25% discount
For more than 10 attendees: 30% discount
To avail the above group discounts, all the participants should register by making a single payment.
Please note that the registration will be closed two days (48 hours) prior to the start date of the seminar.
Call our representative on 1800 447 9407 to have your seats confirmed.
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Contact Information:
Event Coordinator
Toll free: 1800 447 9407
Fax: 302 288 6884
Email: support@globalcompliancepanel.com
Website: https://www.globalcompliancepanel.com
LIVE CHAT SUPPORT- http://www.globalcompliancepanel.com/chat/client.php
GlobalCompliancePanel
NetZealous LLC,
161| Mission Falls Lane| Suite 216, Fremont| CA 94539
About GlobalCompliancepanel
GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.
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