(Canadian Trade Commissioner Service)
Canadian companies that have experience working with regional health authorities in Canada or on the Canadian Health Infoway (CHI) networked projects are well placed to bring their interoperable solutions to the U.S. market.
Did you know that the healthcare industry is receiving $142.3 billion from the U.S. stimulus package? This represents more than any other sector.
Register now to find out how your company can tap into the U.S. Health IT market and become more successful across the border.
Why should you participate?
You will: Discover regional opportunities directly from trade commissioners in Philadelphia and New York; Gain insight on privacy, security, sustainability and interoperability related to the U.S. Health IT industry – What lessons have we learned?; Learn how wireless technology is revolutionizing the delivery of health services.
Date: Wednesday, December 11, 2009 • Time: 1:00 to 2:15 p.m. EST • Cost: Free
After the presentation, there will be a 20-minute Q&A period. The presentation will be in English but the speakers will take questions in both French and English. The presentation will also be made available for on-demand viewing in both French and English following the live webinar. Registration is requested by December 10, 2009. For additional information, please email Guillaume Parent.
Showing posts with label Final Rule. Show all posts
Showing posts with label Final Rule. Show all posts
Thursday, December 3, 2009
Thursday, April 30, 2009
Webinar May 7: Changes in the FDA Prior Notice Final Rule – from the FDA Perspective
NCBFAA Educational Institute
Thursday, May 7, 2009, Noon - 1:30 p.m. ET
Cost: $50.00 per member or non-member participant
1.5 CCS points for attendance
Presented by: FDA
Moderator: Cynthia Allen, Director, NCBFAA Educational Institute
The FDA Prior Notice Final Rule, published November 7, 2008, in the Federal Register, takes effect May 6, 2009. The Final Rule contains significant changes from the Interim Final Rule under which the trade and FDA have been operating.
During the webinar, FDA representatives will address the changes from an operational and regulatory perspective. Compliance with the Final Rule from an automated perspective will be a challenge, as it is anticipated that the changes required in the Customs and Border Protection’s Automated Commercial System (ACS) system will not be complete. The FDA will outline methods to comply with the Final Rule until such changes can be made in ACS.
This is your opportunity to ask the FDA representatives questions about these rule changes and any other FDA import issues.
To participate, go to http://www.ncbfaa.org and select “Changes in the FDA Prior Notice Final Rule” under “Upcoming Events.”
Thursday, May 7, 2009, Noon - 1:30 p.m. ET
Cost: $50.00 per member or non-member participant
1.5 CCS points for attendance
Presented by: FDA
Moderator: Cynthia Allen, Director, NCBFAA Educational Institute
The FDA Prior Notice Final Rule, published November 7, 2008, in the Federal Register, takes effect May 6, 2009. The Final Rule contains significant changes from the Interim Final Rule under which the trade and FDA have been operating.
During the webinar, FDA representatives will address the changes from an operational and regulatory perspective. Compliance with the Final Rule from an automated perspective will be a challenge, as it is anticipated that the changes required in the Customs and Border Protection’s Automated Commercial System (ACS) system will not be complete. The FDA will outline methods to comply with the Final Rule until such changes can be made in ACS.
This is your opportunity to ask the FDA representatives questions about these rule changes and any other FDA import issues.
To participate, go to http://www.ncbfaa.org and select “Changes in the FDA Prior Notice Final Rule” under “Upcoming Events.”
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