RAPS pre-approved webinar on

GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will conduct a RAPS pre-approved webinar on the topic, "Anticipated Changes to the EU Medical Device Directives.

Wilmington, DE (prHWY.com) August 24, 2012 - RAPS pre-approved webinar on "Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees" from GlobalCompliancePanel


Description:A few medical devices directives have been recently planned and are being currently implemented across the EU. This webinar will discuss the specific requirements of these directives, and how they are linked to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.
This course will include specific insight from direct involvement and work within the EU and the European Commission's major improvement objectives to their system today. Areas that are specifically targeted for change will be discussed. This session will also take into consideration the likely implementation timetable.
Attending this webinar offers insight into all these areas and will be helpful for professionals who want to familiarize themselves with or update their working knowledge of these new directives.
-----------------------------------------------------------------------------------------------------------------
When:September 27, 10:00 AM PDT | 01:00 PM EDT
-----------------------------------------------------------------------------------------------------------------
By whom:For the past 9 years, Bob has been President of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding and complying with International Regulations affecting compliance, new product development, manufacturing and quality assurance. RJR has offices in Columbus, OH, Washington DC, and Brussels, Belgium with exclusive affiliates across Asia and Latin America.
Bob has 28 years of past industry experience as a CMC specialist, R&D Director and Global Director of Regulatory Affairs for Merion Merrill Dow pharmaceuticals and Cordis-Dow medical devices. He has a BS/MS degree in Chemistry.
-----------------------------------------------------------------------------------------------------------------
For whom:
The webinar will benefit
o Clinical research and medical operations
o Project Managers
o Product Development personnel
o Manufacturing personnel
o Researchers managing Medical Device R&D and Development
o Quality Assurance such as GMP, GCP Auditors
o Regulatory affairs
o Clinical trial supply personnel
o CRO personnel
o All personnel who need to understand the procedures and impact of placing Medical Devices on the Market across the EU
----------------------------------------------------------------------------------------------------------------
Duration: 90 minutes
-----------------------------------------------------------------------------------------------------------------
To enroll for this webinar, contact
webinars@globalcompliancepanel.com
Phone: 800-447-9407

###

Tag Words: online training, eu medical directives, clinical investigations, clinical evaluations, medical device products

Categories: Health

Press Release Contact
To enroll for this webinar, contact
webinars@globalcompliancepanel.com
Phone: 800-447-9407

Link To This Press Release:

URL HTML Code