Overview of the Medical Device Development and Commercialization Process and Steps for Success
★What cannot be done with animal evaluation and clinical evaluation ★Clear up issues related to regulations such as the Pharmaceutical Affairs Law, GLP, GMP, clinical evaluation, GCP, pharmaceutical applications, and health insurance applications.
Seminar Number S10602 Instructor Takashi Kawabata, Representative of the Medical Device Technology Information Association (Formerly of Nippon Zeon) Target Audience Newcomers and beginners involved in medical device development and commercialization, as well as veterans looking to review. Venue Kawasaki City Industrial Promotion Hall, Conference Room 1 [Kanagawa, Kawasaki Station] - 6 minutes on foot from JR and Keikyu Kawasaki Station Please note that the venue may change to a location in the Tokyo metropolitan area due to scheduled power outages. We will notify you one week prior to the event date. Thank you for your understanding. Date and Time June 16, 2011 (Thursday) 12:30-16:30 Capacity 20 participants - Please apply early as there may be a rush of applications. Participation Fee 49,350 yen (including tax and text costs) for up to 2 participants from one company. *New members who apply for the first time by June 2 will receive an early bird discount price of 44,100 yen. ◆ Early Bird Discount: Please select "1 slot for 2 participants: Early Bird Discount" when registering. ◆ For additional applications from the same organization, an additional 12,600 yen will be charged per participant. ◆ Information on subsidy programs related to seminar participation fees.
- Company：AndTech
- Price：10,000 yen-100,000 yen
