Toronto

Event Profile: The National Franchise & Business Opportunities Show affords an unmatched opportunity for you to meet with, develop strategic partnerships & sell to thousands of small & emerging businesses-all under one roof. Visitor's Profile: Trade Visitors only - marketing & selling persons, franchisee & business opportunity companies, Consumer Commissions etc. Exhibitor's Profile: Profile for exhibit include Small Business Consulting, Legal Services, Financial Advisors, Banking Institutions, Web/Internet Solutions, Government Support, Marketing & Advertising Assistance, Business Associations, IT Support, Business Services, Furniture & Office Supplies, Printers, Accounting & Bookkeeping, Human Resources etc. Organizer: National Event Management, Inc. 60, Renfrew Drive, Suite 105, Markham, Canada. Tel: +(1)-(905)-4772677 Fax: +(1)-(905)-4777872

Event Profile: Canadian International Auto Show (CIAS) is a perfect blend of popular favourites and brand new features. Proven attractions such as the Classic Car Collection and Leisure World are enhanced and improved to deliver even more stopping power. Visitor's Profile: Trade Visitors only - manufacturers, importers & exporters of Vehicle accessories, special equipment, tuning, performance systems, design refinement. Repair & Automotive Services - Equipment for vehicle service and repair, bodywork repair and painting, garage building and management, refuelling and care, disposal and recycling. Exhibitor's Profile: Profile for exhibit include Passenger Cars & Commercial Vehicles, Coach & Auto Bodies Builders, Two & Three Wheelers, Tyres, Car Finance, Insurance & Services Alternative Fuel & Fuel Systems, Auto Accessories, Batteries, Oil & Lubricants, Auto Components, Tools, Garage / Service Station Equipment. Organizer: Canadian International AutoShow 85, Renfrew Drive, Markham, Canada. Tel: +(1)-(905)-9402800 Fax: +(1)-(905)-9402804

Marketing in the 21st century is essentially about customers interacting with brands. In fact, half of the most popular websites in the world are social media. The speed of evolution of the social networking phenomena, and the fundamental changes it has brought about in the consumer-marketer relationship, has caught most marketers off guard. In these new, potent social spaces, average citizens are empowered to communicate directly, and effectively, with marketers. Marketers are vividly aware of the potential damage, or good, consumer sentiment in virtual space can have on their brands, their reputations and their bottom line. This conference will address ways in which the richness of information, dialogue and consumer insight inherent in social networks can be organized and drawn upon to further our understanding of consumer interactivity with brands.

A Two-Day Comprehensive & Interactive Course with Workshops on: - FDA's Center for Devices and Radiological Health Investigations - Clarifying FDA Classification of Medical Devices - Memoranda of Understanding (MOU) - Developing QSR/GMP/ISO for combo products - Principals of ICH GCP for Medical Devices - Definitions and Classifications of Medical Device - The Premarket Notification (510K) Summaries and Reviews - Investigational Device Exemption (IDE) Applications - Premarket Approval (PMA) Review Process - Safety and Effectiveness Requirements - Humanitarian Device Exemption (HDE) - Post Market Obligations - Managing Recalls and Problem Reporting - Planning and Implementing an Clinical Audit - Determining a Regulatory Strategy - Clinical Trials for Medical Devices - Sponsor Obligations - Inspection and Audit of Vendors - FDA Notification procedures Distinguished Course Leaders Martha A. Feldman, RAC President & CEO Drug & Device Development Co., Inc. Albert A. Ghignone, MS, RAC CEO AAG Incorporated

An Important Two-Day Comprehensive & Interactive Seminar with Case Studies and Workshops On: - FDA, Today and Tomorrow - FDA Rules and Regulations - FDA’s Initiative on Pharmaceutical cGMPs for the 21st Century - Application and Approval in the US - FDA Inspections - FDA Pre-Approval Inspectional Program Before, During and After - System Based Inspections Quality, Facility & Equipment, Materials, Production, Packaging/Labeling, Lab Controls - A Quality Systems Approach to GMPs - Most Common GMP Deficiencies by Systems - Expectations for cGMPs for Laboratories - Inspections of Combination Devices - Requirements for Inspection Preparations - Surviving an US FDA Audit - Criteria for Warning Letter vs Violation Letter - Responding to FDA FD-483 Distinguished Course Leaders Ms. Maxine Fritz Vice President, Pharmaceutical Quality Systems and Validation Quintiles Consulting Mr. John Godshalk Senior Consultant Biologics Consulting Group Dr. Marla Phillips Senior Compliance Consultant