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Events & ProgramsMontreal - EU Standards Certification Seminar on Medical Devices, 7:30am - 3:30pm
Date:
8 October 2008
Description:
Séminaire sur les normes et la certification européenne pour les appareils médicaux (EN ANGLAIS)Comment qualifier avec succès votre appareil pour le marché européen. Quand: Le 8 octobre, 2008, de 7:00 à 16:00 Où :Institut des matériaux industriels, Conseil de recherche national du Canada 75, boul. de Mortagne, Boucherville Quoi:L’Union européenne a récemment adopté des règles et normes communes pour les appareils médicaux. Ce séminaire sera le premier auquel le Gouvernement du Canada a convié un expert, Harold Rentschler, président de Medical Device Certification GmbH (www.mdc-ce.de) pour offrir une vue d’ensemble du nouveau système règlementaire européen. Son expérience vous permettra d’acquérir le savoir-faire requis afin d’obtenir les certifications requises pour votre appareil médical en préparation de son exportation vers le marché européen. Il s’agira d’un séminaire interactif d’une journée complète auquel seront servis un petit-déjeuner, un déjeuner ainsi que des rafraîchissements. Vous aurez également la possibilité de poser les questions qui vous préoccupent au sujet de votre appareil ou technologie médicale. Pour s’enregistrer: Pour de plus amples informations: Elise Racicot I Déléguée commerciale Service des délégués commerciaux Affaires étrangères et commerce international Canada Tél: 514-496-4568 I Fax: 514-283-8794
Hosted By: The Canadian Trade Commissioners Service Department and MEDEC with the support of the National Research Council of Canada and the collaboration of the Campus des technologies de la santé. The European Union recently adopted common regulatory standards for medical devices. This seminar will be the first where an expert has been invited by the Government of Canada to provide Medical Device businesses with an overview of the new EU Regulatory system, Harold Rentschler, President of Medical Device Certification GmbH (www.mdc-ce.de). His experience will give you the know-how needed to systematically seek regulatory approval of your medical device preparatory to exporting to the EU market. This will be an interactive full day seminar where breakfast, lunch and refreshments will be served. You will be able to ask questions that are specific to your technology or device. Additional information: Elise Racicot I Trade Commissioner, Health Industries Trade Commissioner ServiceForeign Affairs and International Trade CanadaTél: 514-496-4568 I Fax: 514-283-8794 elise.racicot@international.gc.ca **PLEASE NOTE WE ONLY ACCEPT VISA AND MC **
Location:
Industrial Materials Institute, National Research Council of Canada 75, boul, de Mortagne, Boucherville
Edmonton - EU Standards Certification Seminar on Medical Devices, 7:30am - 3:30pm
Date:
9 October 2008
Description:
Hosted By: "The Canadian Trade Commissioner Services, MEDEC and the Alberta Health Industry Association with the support of the Government of Alberta." The European Union recently adopted common regulatory standards for medical devices. This seminar will be the first where an expert has been invited by the Government of Canada to provide Medical Device businesses with an overview of the new EU Regulatory system, Harold Rentschler, President of Medical Device Certification GmbH (www.mdc-ce.de). His experience will give you the know-how needed to systematically seek regulatory approval of your medical device preparatory to exporting to the EU market. This will be an interactive full day seminar where breakfast, lunch and refreshments will be served. You will be able to ask questions that are specific to your technology or device. Additional information: Chris Mack I Trade Commissioner, Regional Office of the Trade Commissioner Service , Prairie and Northern Region, Foreign Affairs and International Tel: 780-495-3060 I Fax: 780-495-4507 christopher.mack@international.gc.ca **PLEASE NOTE WE ONLY ACCEPT VISA AND MC **
Location:
Royal Mayfair Golf and Country Club , 9450 Groat Road, Edmonton
MEDEC Legal & Regulatory Conference
Date:
29 October 2008 - 30 October 2008
Description:
MEDEC’s not-to-be-missed annual legal and regulatory learning and networking event! Features public and private industry experts speaking and engaging in interactive workshops on current and future scenarios as they apply to medical devices and emerging technologies across jurisdictions. Who should Attend? - Regulatory Affairs Associates of all levels - QA Managers/Associates - Legal Counsel - Marketing Directors - Marketing Associates - Product Managers - Business Development Associates - General Managers REGISTRATION INCLUDES: Two days of Speakers, Workshops, Breakfast, Lunch and Refreshments Please note: Early-bird special: Save $100 when you register by Sept. 26 **PLEASE NOTE WE ONLY ACCEPT VISA AND MC ** **Cancellations must be received by October 15 in order to receive a refund. Cancellations received after October 15 will receive a credit towards a future MEDEC event**
Location:
Toronto Congress Centre
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