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Global Medical Device Regulation
Global Medical Device Regulation
This seminar provides a basic description of global regulatory strategy for medical devices and offers an overview of international medical device regulations. Country-specific regulatory requirements for Canada, EU.
Fremont,
California,
United States
(sardnews.org)
31/07/2014
Summary: GlobalCompliancePanel will organize a RAPS-approved two-day, in-person seminar in Denver, CO on the topic, “Global Medical Device Regulation” on July 31 and August 1, 2014 (Thursday & Friday). Dr. Thomas E. Colonna, who provides consulting services in the scientific and regulatory fields, will be the speaker at this session.
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 31 and August 1, 2014 from 9 A.M to 5 P.M, is Hotel Hilton Garden Inn Denver Downtown 1400 Welton St, Denver, CO 80202.
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What the seminar is about:
Countries around the world have their own, unique regulatory requirements for medical devices. For medical device companies, it is important to understand the way each country or bloc operates.
This seminar provides a basic description of global regulatory strategy for medical devices and offers an overview of international medical device regulations. Country-specific regulatory requirements for Canada, EU, and US are included in this course.
The speaker will begin with a discussion of the similarity of global requirements, including both voluntary and mandatory standards and directives, and progresses to in-depth analyses of market specific requirements.
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About the Speaker:
Thomas E. Colonna earned a bachelor of science in microbiology from the University of Sciences in Philadelphia (formerly the Philadelphia College of Pharmacy and Science), a Ph.D. in molecular biology from the Johns Hopkins University, and a law degree from the Georgetown University Law Center. In addition, Dr. Colonna holds academic appointments at Johns Hopkins University and the University of Sciences in Philadelphia.
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For whom:
This seminar will benefit:
o Regulatory professionals working in the medical device field
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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. GCP offers a broad range of high quality regulatory and compliance-related services relating to Medical Devices, Pharmaceutical, FDA, Food, PCI industries, and SOX. Some of the Governing Areas its webinars cover are GxP (Manufacturing/Clinical/Lab), EU and ISO.
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Price:
Register now and save $200. (Early Bird)
Until July 18: Early Bird Price: $1,295.00.
From July 19 to 29: 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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