Events Tagged "seminar"

Working Effectively with Indians

A One-Day Seminar in New York, November 14, 2006 ·Understand Indian culture and workstyle ·Learn how to best communicate with Indians ·Increase efficiency and effectiveness

Information Architecture 3.0

As we venture beyond Web 2.0, how do we reconcile the timeless principles of design and organization with new models of interaction? Come explore this question in a seminar with Peter Morville.

(4 days)

UI12 - User Interface 12 Conference

User Interface 12 is being held November 5-8, 2007 in Cambridge, MA. We've lined up fantastic speakers giving full-day seminars and short talks on today's most pressing usability and design issues.

Architect as DEVELOPER

Jonathan Segal FAIA will teach attendees to break free from the client and develop their own futures!!

(3 days)

2nd Seminar on Usability and Accessibility MEXICO

Join the Second International Seminar on Usability and Accessibility for the Web in Monterrey, Mexico

(2 days)

Cooper Hosts Innovation Games Class

Luke Hohmann, author of "Innovation Games: Creating Breakthrough Products Through Collaborative Play" will teach an intensive class about Innovation Games, March 30-31, 2009 at Cooper in SF CA.

Clear as Mud: Obtaining & Marketing your 510(K)

An interactive workshop to ensure you understand how to obtain a 510(k) in today's environment at FDA.

(4 days)

UX Intensive 2011 Chicago

Adaptive Path's 4-day workshop for experienced professionals. Learn key elements of successful interactive experiences: Design Strategy, Design Research, Information Architecture & Interaction Design.

Medical Device Complaints, MDR’s and Recalls

This webinar will discuss in detail the FDA regulations and the regulatory process with respect to medical device complaint handling and reporting.

Harmonized Tariff Schedule and Schedule B

This full-day seminar will provide comprehensive information on how to classify products under the Harmonized Tariff Schedule (HTS) and Schedule B using the General Rules of Interpretation.

NAFTA Rules of Origin and Documentation

It is required for most goods that qualify under the rules and must be completed by the exporter and in possession of the importer when the goods are entered into the importing country.

FDA Warning Letter - Consent Software Validation

This FDA warning letter will discuss what to do to avoid additional software related compliance along with the response steps where the citations that directly or indirectly include automated system.

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